Linked Data
ClinVar Variation Id:
4431
dbSNP Id:
rs104894103
ExAC:
9:32974493 C / T
gnomAD v2:
9-32974493-C-T
gnomAD v3:
9-32974495-C-T
gnomAD v4:
9-32974495-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.32974495C>T , CM000671.2:g.32974495C>T | GRCh38 |
| NC_000009.11:g.32974493C>T , CM000671.1:g.32974493C>T | GRCh37 |
| NC_000009.10:g.32964493C>T | NCBI36 |
| NG_012821.1:g.32134G>A | |
| NG_012821.2:g.55637G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309615.8:c.675G>A | ENSP00000311547.4:p.Trp225Ter | |
| ENST00000379817.7:c.837G>A MANE Select | ENSP00000369145.2:p.Trp279Ter | |
| ENST00000379819.6:c.837G>A | ENSP00000369147.2:p.Trp279Ter | |
| ENST00000379825.7:c.837G>A | ENSP00000369153.3:p.Trp279Ter | |
| ENST00000397172.8:c.621G>A | ENSP00000380357.4:p.Trp207Ter | |
| ENST00000436040.7:c.675G>A | ENSP00000400806.4:p.Trp225Ter | |
| ENST00000460940.6:c.*455G>A | ENSP00000418311.1:n.*455G>A | |
| ENST00000463596.6:c.837G>A | ENSP00000419846.1:p.Trp279Ter | |
| ENST00000465003.6:c.*567G>A | ENSP00000419430.2:n.*567G>A | |
| ENST00000467331.6:c.*682G>A | ENSP00000418733.1:n.*682G>A | |
| ENST00000468275.6:c.837G>A | ENSP00000420263.2:p.Trp279Ter | |
| ENST00000472896.6:c.*631G>A | ENSP00000417804.2:n.*631G>A | |
| ENST00000474658.7:c.*280G>A | ENSP00000417750.3:n.*280G>A | |
| ENST00000476858.6:c.675G>A | ENSP00000419042.2:p.Trp225Ter | |
| ENST00000477119.2:c.720G>A | ENSP00000417649.2:p.Trp240Ter | |
| ENST00000479656.6:c.*682G>A | ENSP00000420071.1:n.*682G>A | |
| ENST00000482687.6:c.*455G>A | ENSP00000419289.2:n.*455G>A | |
| ENST00000483148.6:c.*464G>A | ENSP00000419723.1:n.*464G>A | |
| ENST00000485479.6:c.*558G>A | ENSP00000418144.1:n.*558G>A | |
| ENST00000495360.6:c.*580G>A | ENSP00000419623.2:n.*580G>A | |
| ENST00000671774.1:n.830G>A | ||
| ENST00000671912.1:c.*31G>A | ENSP00000500871.1:n.*31G>A | |
| ENST00000672152.1:n.807G>A | ||
| ENST00000672244.1:c.*31G>A | ENSP00000499875.1:n.*31G>A | |
| ENST00000672281.1:n.1034G>A | ||
| ENST00000672286.1:n.1098G>A | ||
| ENST00000672438.1:c.573G>A | ENSP00000499997.1:p.Trp191Ter | |
| ENST00000672476.1:n.1029G>A | ||
| ENST00000672493.1:n.1376G>A | ||
| ENST00000672519.1:c.*388+11476G>A | ENSP00000500320.1:n.*388+11476G>A | |
| ENST00000672535.1:c.*567G>A | ENSP00000499872.1:n.*567G>A | |
| ENST00000672615.1:n.914G>A | ||
| ENST00000672846.1:c.*567G>A | ENSP00000500396.1:n.*567G>A | |
| ENST00000673171.1:n.687G>A | ||
| ENST00000673181.1:n.1407G>A | ||
| ENST00000673211.1:n.919G>A | ||
| ENST00000673248.1:c.573G>A | ENSP00000500601.1:p.Trp191Ter | |
| ENST00000673333.1:n.1115G>A | ||
| ENST00000673360.1:c.*280G>A | ENSP00000500360.1:n.*280G>A | |
| ENST00000673416.1:c.573G>A | ENSP00000500738.1:p.Trp191Ter | |
| ENST00000673485.1:n.1034G>A | ||
| ENST00000673487.1:c.*567G>A | ENSP00000500943.1:n.*567G>A | |
| ENST00000673598.1:c.315G>A | ENSP00000499991.1:p.Trp105Ter | |
| ENST00000309615.7:c.675G>A | ENSP00000311547.4:p.Trp225Ter | |
| ENST00000379813.7:c.819G>A | ENSP00000369141.4:p.Trp273Ter | |
| ENST00000379817.6:c.837G>A | ENSP00000369145.2:p.Trp279Ter | |
| ENST00000379819.5:c.879G>A | ENSP00000369147.1:p.Trp293Ter | |
| ENST00000379825.6:c.879G>A | ENSP00000369153.2:p.Trp293Ter | |
| ENST00000397172.7:c.663G>A | ENSP00000380357.3:p.Trp221Ter | |
| ENST00000436040.6:c.837G>A | ENSP00000400806.3:p.Trp279Ter | |
| ENST00000460940.5:c.*455G>A | ENSP00000418311.1:n.*455G>A | |
| ENST00000463596.5:c.837G>A | ENSP00000419846.1:p.Trp279Ter | |
| ENST00000465003.5:c.*464G>A | ENSP00000419430.1:n.*464G>A | |
| ENST00000467331.5:c.*682G>A | ENSP00000418733.1:n.*682G>A | |
| ENST00000468275.5:c.837G>A | ENSP00000420263.1:p.Trp279Ter | |
| ENST00000472896.5:c.*340G>A | ENSP00000417804.1:n.*340G>A | |
| ENST00000474658.6:c.504G>A | ||
| ENST00000476858.5:c.717G>A | ENSP00000419042.1:p.Trp239Ter | |
| ENST00000479656.5:c.*682G>A | ENSP00000420071.1:n.*682G>A | |
| ENST00000482687.5:c.*31G>A | ENSP00000419289.1:n.*31G>A | |
| ENST00000483148.5:c.*237G>A | ENSP00000419723.1:n.*237G>A | |
| ENST00000485479.5:c.*567G>A | ENSP00000418144.1:n.*567G>A | |
| ENST00000494649.5:c.*682G>A | ENSP00000417634.1:n.*682G>A | |
| ENST00000495360.5:c.*567G>A | ENSP00000419623.1:n.*567G>A | |
| NM_001195248.1:c.879G>A | NP_001182177.1:p.Trp293Ter | |
| NM_001195249.1:c.837G>A | NP_001182178.1:p.Trp279Ter | |
| NM_001195250.1:c.717G>A | NP_001182179.1:p.Trp239Ter | |
| NM_001195251.1:c.837G>A | NP_001182180.1:p.Trp279Ter | |
| NM_001195252.1:c.663G>A | NP_001182181.1:p.Trp221Ter | |
| NM_001195254.1:c.675G>A | NP_001182183.1:p.Trp225Ter | |
| NM_175069.2:c.879G>A | NP_778239.1:p.Trp293Ter | |
| NM_175073.2:c.837G>A | NP_778243.1:p.Trp279Ter | |
| NR_036576.1:n.911G>A | ||
| NR_036577.1:n.801G>A | ||
| NR_036578.1:n.933G>A | ||
| NR_036579.1:n.1080G>A | ||
| XM_006716791.2:c.837G>A | XP_006716854.1:p.Trp279Ter | |
| XM_006716792.2:c.573G>A | XP_006716855.1:p.Trp191Ter | |
| XM_011517936.1:c.573G>A | XP_011516238.1:p.Trp191Ter | |
| XM_011517937.1:c.573G>A | XP_011516239.1:p.Trp191Ter | |
| XM_011517938.1:c.573G>A | XP_011516240.1:p.Trp191Ter | |
| XM_011517939.1:c.573G>A | XP_011516241.1:p.Trp191Ter | |
| XR_428423.2:n.689G>A | ||
| XR_929276.1:n.1288G>A | ||
| XR_929277.1:n.1311G>A | ||
| XR_929279.1:n.689G>A | ||
| XM_006716791.4:c.837G>A | XP_006716854.1:p.Trp279Ter | |
| XM_006716792.3:c.573G>A | XP_006716855.1:p.Trp191Ter | |
| XM_011517938.2:c.573G>A | XP_011516240.1:p.Trp191Ter | |
| XM_011517939.3:c.573G>A | XP_011516241.1:p.Trp191Ter | |
| XM_017014831.1:c.813-7722G>A | XP_016870320.1:n.813-7722G>A | |
| XM_017014832.1:c.813-7722G>A | XP_016870321.1:n.813-7722G>A | |
| XM_017014833.2:c.813-7722G>A | XP_016870322.1:n.813-7722G>A | |
| XM_017014836.2:c.813-7722G>A | XP_016870325.1:n.813-7722G>A | |
| XM_017014837.2:c.675G>A | XP_016870326.1:p.Trp225Ter | |
| XM_017014838.1:c.573G>A | XP_016870327.1:p.Trp191Ter | |
| XM_024447575.1:c.837G>A | XP_024303343.1:p.Trp279Ter | |
| XM_024447576.1:c.837G>A | XP_024303344.1:p.Trp279Ter | |
| XM_024447577.1:c.837G>A | XP_024303345.1:p.Trp279Ter | |
| XM_024447578.1:c.813-7722G>A | XP_024303346.1:n.813-7722G>A | |
| XM_024447579.1:c.837G>A | XP_024303347.1:p.Trp279Ter | |
| XM_024447580.1:c.675G>A | XP_024303348.1:p.Trp225Ter | |
| XM_024447581.1:c.573G>A | XP_024303349.1:p.Trp191Ter | |
| XM_024447582.1:c.573G>A | XP_024303350.1:p.Trp191Ter | |
| XR_001746325.2:n.1311G>A | ||
| XR_001746326.2:n.1296G>A | ||
| XR_428423.3:n.689G>A | ||
| XR_929276.3:n.1288G>A | ||
| XR_929277.3:n.1311G>A | ||
| NM_001195248.2:c.837G>A MANE Select | NP_001182177.2:p.Trp279Ter | |
| NM_001195250.2:c.675G>A | NP_001182179.2:p.Trp225Ter | |
| NM_001195252.2:c.621G>A | NP_001182181.2:p.Trp207Ter | |
| NM_001368995.1:c.837G>A | NP_001355924.1:p.Trp279Ter | |
| NM_001368996.1:c.837G>A | NP_001355925.1:p.Trp279Ter | |
| NM_001368997.1:c.837G>A | NP_001355926.1:p.Trp279Ter | |
| NM_001368998.1:c.837G>A | NP_001355927.1:p.Trp279Ter | |
| NM_001368999.1:c.837G>A | NP_001355928.1:p.Trp279Ter | |
| NM_001369000.1:c.675G>A | NP_001355929.1:p.Trp225Ter | |
| NM_001369001.1:c.675G>A | NP_001355930.1:p.Trp225Ter | |
| NM_001369002.1:c.573G>A | NP_001355931.1:p.Trp191Ter | |
| NM_001369003.1:c.573G>A | NP_001355932.1:p.Trp191Ter | |
| NM_001369004.1:c.573G>A | NP_001355933.1:p.Trp191Ter | |
| NM_001369005.1:c.573G>A | NP_001355934.1:p.Trp191Ter | |
| NM_001369006.1:c.573G>A | NP_001355935.1:p.Trp191Ter | |
| NM_001370669.1:c.573G>A | NP_001357598.1:p.Trp191Ter | |
| NM_001370670.1:c.573G>A | NP_001357599.1:p.Trp191Ter | |
| NM_001370673.1:c.573G>A | NP_001357602.1:p.Trp191Ter | |
| NM_175069.3:c.837G>A | NP_778239.2:p.Trp279Ter | |
| NR_160920.1:n.676G>A | ||
| NR_160921.1:n.807G>A | ||
| NR_160922.1:n.1038G>A | ||
| NR_160923.1:n.842G>A | ||
| NR_160924.1:n.847G>A | ||
| NR_160925.1:n.1043G>A | ||
| NR_160926.1:n.833G>A | ||
| NR_160927.1:n.926G>A | ||
| NR_160928.1:n.816G>A | ||
| NR_160929.1:n.730G>A | ||
| NR_160930.1:n.783G>A | ||
| NR_160931.1:n.1022G>A | ||
| NM_001195249.2:c.837G>A | NP_001182178.1:p.Trp279Ter | |
| NM_001195251.2:c.837G>A | NP_001182180.1:p.Trp279Ter | |
| NM_001195254.2:c.675G>A | NP_001182183.1:p.Trp225Ter | |
| NM_175073.3:c.837G>A | NP_778243.1:p.Trp279Ter | |
| NR_036577.2:n.788G>A |