UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Linked Data
dbSNP Id:
rs9371601
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152469438G>A , CM000668.2:g.152469438G>A | GRCh38 |
| NC_000006.11:g.152790573G>A , CM000668.1:g.152790573G>A | GRCh37 |
| NC_000006.10:g.152832266G>A | NCBI36 |
| NG_012855.1:g.172962C>T | |
| NG_012855.2:g.172962C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367255.10:c.1632+2159C>T MANE Select | ENSP00000356224.5:n.1632+2159C>T | |
| ENST00000423061.6:c.1653+2159C>T | ENSP00000396024.1:n.1653+2159C>T | |
| ENST00000535896.7:c.1626+2159C>T | ENSP00000500235.1:n.1626+2159C>T | |
| ENST00000672122.1:c.1575+2159C>T | ENSP00000500559.1:n.1575+2159C>T | |
| ENST00000673163.1:c.*1602+2159C>T | ENSP00000499934.1:n.*1602+2159C>T | |
| ENST00000673281.1:c.1626+2159C>T | ENSP00000500893.1:n.1626+2159C>T | |
| ENST00000341594.9:c.1602+2159C>T | ENSP00000341887.6:n.1602+2159C>T | |
| ENST00000367248.7:c.1602+2159C>T | ENSP00000356217.3:n.1602+2159C>T | |
| ENST00000367253.8:c.1632+2159C>T | ENSP00000356222.4:n.1632+2159C>T | |
| ENST00000367255.9:c.1632+2159C>T | ENSP00000356224.5:n.1632+2159C>T | |
| ENST00000413186.6:c.1632+2159C>T | ENSP00000414510.2:n.1632+2159C>T | |
| ENST00000423061.5:c.1653+2159C>T | ENSP00000396024.1:n.1653+2159C>T | |
| ENST00000461872.6:n.1850+2159C>T | ||
| ENST00000466159.6:c.1632+2159C>T | ENSP00000446021.1:n.1632+2159C>T | |
| ENST00000468937.2:n.388+2159C>T | ||
| ENST00000474655.6:c.234+2159C>T | ||
| ENST00000481502.5:n.243+2159C>T | ||
| ENST00000495090.6:c.333+2159C>T | ENSP00000438508.1:n.333+2159C>T | |
| ENST00000535896.6:n.452+2159C>T | ||
| ENST00000537750.5:c.1581+2159C>T | ENSP00000441264.1:n.1581+2159C>T | |
| NM_033071.3:c.1653+2159C>T | NP_149062.1:n.1653+2159C>T | |
| NM_182961.3:c.1632+2159C>T | NP_892006.3:n.1632+2159C>T | |
| XM_006715407.1:c.1653+2159C>T | XP_006715470.1:n.1653+2159C>T | |
| XM_006715408.1:c.1653+2159C>T | XP_006715471.1:n.1653+2159C>T | |
| XM_006715409.1:c.1632+2159C>T | XP_006715472.1:n.1632+2159C>T | |
| XM_006715410.1:c.1653+2159C>T | XP_006715473.1:n.1653+2159C>T | |
| XM_006715411.1:c.1602+2159C>T | XP_006715474.1:n.1602+2159C>T | |
| XM_006715412.1:c.1653+2159C>T | XP_006715475.1:n.1653+2159C>T | |
| XM_006715413.1:c.1653+2159C>T | XP_006715476.1:n.1653+2159C>T | |
| XM_006715414.1:c.1581+2159C>T | XP_006715477.1:n.1581+2159C>T | |
| XM_006715415.1:c.1653+2159C>T | XP_006715478.1:n.1653+2159C>T | |
| XM_006715416.1:c.1653+2159C>T | XP_006715479.1:n.1653+2159C>T | |
| XM_006715417.1:c.1653+2159C>T | XP_006715480.1:n.1653+2159C>T | |
| XM_006715420.1:c.1653+2159C>T | XP_006715483.1:n.1653+2159C>T | |
| XM_006715421.1:c.1653+2159C>T | XP_006715484.1:n.1653+2159C>T | |
| XM_006715422.1:c.1653+2159C>T | XP_006715485.1:n.1653+2159C>T | |
| XM_006715423.1:c.1653+2159C>T | XP_006715486.1:n.1653+2159C>T | |
| XM_006715424.1:c.1653+2159C>T | XP_006715487.1:n.1653+2159C>T | |
| XM_006715425.1:c.1653+2159C>T | XP_006715488.1:n.1653+2159C>T | |
| XM_011535641.1:c.1653+2159C>T | XP_011533943.1:n.1653+2159C>T | |
| XM_011535642.1:c.1653+2159C>T | XP_011533944.1:n.1653+2159C>T | |
| XM_011535643.1:c.1653+2159C>T | XP_011533945.1:n.1653+2159C>T | |
| XM_011535644.1:c.-73+2159C>T | XP_011533946.1:n.-73+2159C>T | |
| XM_011535646.1:c.1653+2159C>T | XP_011533948.1:n.1653+2159C>T | |
| XM_006715408.2:c.1653+2159C>T | XP_006715471.1:n.1653+2159C>T | |
| XM_006715410.2:c.1653+2159C>T | XP_006715473.1:n.1653+2159C>T | |
| XM_006715412.2:c.1653+2159C>T | XP_006715475.1:n.1653+2159C>T | |
| XM_006715413.2:c.1653+2159C>T | XP_006715476.1:n.1653+2159C>T | |
| XM_006715415.2:c.1653+2159C>T | XP_006715478.1:n.1653+2159C>T | |
| XM_006715416.2:c.1653+2159C>T | XP_006715479.1:n.1653+2159C>T | |
| XM_006715417.2:c.1653+2159C>T | XP_006715480.1:n.1653+2159C>T | |
| XM_006715420.2:c.1653+2159C>T | XP_006715483.1:n.1653+2159C>T | |
| XM_006715421.2:c.1653+2159C>T | XP_006715484.1:n.1653+2159C>T | |
| XM_006715423.2:c.1653+2159C>T | XP_006715486.1:n.1653+2159C>T | |
| XM_006715424.2:c.1653+2159C>T | XP_006715487.1:n.1653+2159C>T | |
| XM_006715425.2:c.1653+2159C>T | XP_006715488.1:n.1653+2159C>T | |
| XM_011535641.2:c.1653+2159C>T | XP_011533943.1:n.1653+2159C>T | |
| XM_011535642.2:c.1653+2159C>T | XP_011533944.1:n.1653+2159C>T | |
| XM_017010608.1:c.1653+2159C>T | XP_016866097.1:n.1653+2159C>T | |
| XM_017010609.1:c.1653+2159C>T | XP_016866098.1:n.1653+2159C>T | |
| XM_017010610.1:c.1632+2159C>T | XP_016866099.1:n.1632+2159C>T | |
| XM_017010611.2:c.1626+2159C>T | XP_016866100.1:n.1626+2159C>T | |
| XM_017010612.1:c.1575+2159C>T | XP_016866101.1:n.1575+2159C>T | |
| XM_017010613.1:c.1653+2159C>T | XP_016866102.1:n.1653+2159C>T | |
| XM_017010614.1:c.1653+2159C>T | XP_016866103.1:n.1653+2159C>T | |
| XM_017010615.1:c.1653+2159C>T | XP_016866104.1:n.1653+2159C>T | |
| XM_017010616.1:c.1653+2159C>T | XP_016866105.1:n.1653+2159C>T | |
| XM_017010617.1:c.1653+2159C>T | XP_016866106.1:n.1653+2159C>T | |
| XM_017010618.1:c.1653+2159C>T | XP_016866107.1:n.1653+2159C>T | |
| XM_017010619.1:c.-73+2159C>T | XP_016866108.1:n.-73+2159C>T | |
| XR_001743287.1:n.2136+2159C>T | ||
| NM_182961.4:c.1632+2159C>T MANE Select | NP_892006.3:n.1632+2159C>T | |
| NM_033071.5:c.1653+2159C>T | NP_149062.2:n.1653+2159C>T |