Linked Data
ClinVar Variation Id:
11236
ClinVar RCV Id:
RCV003151720
dbSNP Id:
rs104894788
PubMed:
PMID:8817332
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.31180437C>T , CM000685.2:g.31180437C>T | GRCh38 |
| NC_000023.10:g.31198554C>T , CM000685.1:g.31198554C>T | GRCh37 |
| NC_000023.9:g.31108475C>T | NCBI36 |
| NG_012232.1:g.2164173G>A , LRG_199:g.2164173G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000358062.7:c.4865G>A | ENSP00000350765.3:p.Cys1622Tyr | |
| ENST00000475732.3:n.2366G>A | ||
| ENST00000680162.2:c.815G>A | ENSP00000506634.2:p.Cys272Tyr | |
| ENST00000680768.2:c.815G>A | ENSP00000506359.2:p.Cys272Tyr | |
| ENST00000681989.1:n.817G>A | ||
| ENST00000682238.1:c.2639G>A | ENSP00000508124.1:p.Cys880Tyr | |
| ENST00000682322.1:c.815G>A | ENSP00000507690.1:p.Cys272Tyr | |
| ENST00000682600.1:c.815G>A | ENSP00000507640.1:p.Cys272Tyr | |
| ENST00000682769.1:n.650G>A | ||
| ENST00000683509.1:n.1536G>A | ||
| ENST00000683675.1:n.1118G>A | ||
| ENST00000683709.1:n.1537G>A | ||
| ENST00000683957.1:n.3511G>A | ||
| ENST00000684130.1:c.2639G>A | ENSP00000508037.1:p.Cys880Tyr | |
| ENST00000343523.7:c.1874G>A | ENSP00000340057.4:p.Cys625Tyr | |
| ENST00000357033.9:c.10019G>A MANE Select | ENSP00000354923.3:p.Cys3340Tyr | |
| ENST00000475732.2:n.385G>A | ||
| ENST00000619831.5:c.5987G>A | ENSP00000479270.2:p.Cys1996Tyr | |
| ENST00000620040.5:c.2639G>A | ENSP00000478150.2:p.Cys880Tyr | |
| ENST00000679641.1:c.*21G>A | ENSP00000506135.1:n.*21G>A | |
| ENST00000680162.1:c.692G>A | ENSP00000506634.1:p.Cys231Tyr | |
| ENST00000680355.1:c.815G>A | ENSP00000506257.1:p.Cys272Tyr | |
| ENST00000680557.1:c.603+23524G>A | ENSP00000505164.1:n.603+23524G>A | |
| ENST00000680768.1:c.758G>A | ENSP00000506359.1:p.Cys253Tyr | |
| ENST00000680961.1:c.*21G>A | ENSP00000506386.1:n.*21G>A | |
| ENST00000681153.1:c.815G>A | ENSP00000505124.1:p.Cys272Tyr | |
| ENST00000681654.1:n.949G>A | ||
| ENST00000343523.6:c.1832G>A | ENSP00000340057.3:p.Cys611Tyr | |
| ENST00000357033.8:c.10019G>A | ENSP00000354923.3:p.Cys3340Tyr | |
| ENST00000358062.6:c.3107G>A | ENSP00000350765.2:p.Cys1036Tyr | |
| ENST00000359836.5:c.2639G>A | ENSP00000352894.1:p.Cys880Tyr | |
| ENST00000361471.8:c.815G>A | ENSP00000354464.4:p.Cys272Tyr | |
| ENST00000378677.6:c.10007G>A | ENSP00000367948.2:p.Cys3336Tyr | |
| ENST00000378680.6:c.815G>A | ENSP00000367951.2:p.Cys272Tyr | |
| ENST00000378702.8:c.815G>A | ENSP00000367974.4:p.Cys272Tyr | |
| ENST00000378705.3:c.389G>A | ENSP00000367977.3:p.Cys130Tyr | |
| ENST00000378707.7:c.2639G>A | ENSP00000367979.3:p.Cys880Tyr | |
| ENST00000378723.7:c.815G>A | ENSP00000367997.3:p.Cys272Tyr | |
| ENST00000474231.5:c.2639G>A | ENSP00000417123.1:p.Cys880Tyr | |
| ENST00000475732.1:n.235G>A | ||
| ENST00000541735.5:c.2639G>A | ENSP00000444119.1:p.Cys880Tyr | |
| ENST00000619831.4:c.10004G>A | ENSP00000479270.1:p.Cys3335Tyr | |
| ENST00000620040.4:c.10016G>A | ENSP00000478150.1:p.Cys3339Tyr | |
| NM_000109.3:c.9995G>A | NP_000100.2:p.Cys3332Tyr | |
| NM_004006.2:c.10019G>A , LRG_199t1:c.10019G>A | NP_003997.1:p.Cys3340Tyr | |
| NM_004009.3:c.10007G>A | NP_004000.1:p.Cys3336Tyr | |
| NM_004010.3:c.9650G>A | NP_004001.1:p.Cys3217Tyr | |
| NM_004011.3:c.5996G>A | NP_004002.2:p.Cys1999Tyr | |
| NM_004012.3:c.5987G>A | NP_004003.1:p.Cys1996Tyr | |
| NM_004013.2:c.2639G>A | NP_004004.1:p.Cys880Tyr | |
| NM_004014.2:c.1832G>A | NP_004005.1:p.Cys611Tyr | |
| NM_004015.2:c.815G>A | NP_004006.1:p.Cys272Tyr | |
| NM_004016.2:c.815G>A | NP_004007.1:p.Cys272Tyr | |
| NM_004017.2:c.815G>A | NP_004008.1:p.Cys272Tyr | |
| NM_004018.2:c.815G>A | NP_004009.1:p.Cys272Tyr | |
| NM_004019.2:c.815G>A | NP_004010.1:p.Cys272Tyr | |
| NM_004020.3:c.2639G>A | NP_004011.2:p.Cys880Tyr | |
| NM_004021.2:c.2639G>A | NP_004012.1:p.Cys880Tyr | |
| NM_004022.2:c.2639G>A | NP_004013.1:p.Cys880Tyr | |
| NM_004023.2:c.2639G>A | NP_004014.1:p.Cys880Tyr | |
| XM_006724468.2:c.10019G>A | XP_006724531.1:p.Cys3340Tyr | |
| XM_006724469.2:c.9995G>A | XP_006724532.1:p.Cys3332Tyr | |
| XM_006724470.2:c.10019G>A | XP_006724533.1:p.Cys3340Tyr | |
| XM_006724471.2:c.10019G>A | XP_006724534.1:p.Cys3340Tyr | |
| XM_006724472.2:c.9890G>A | XP_006724535.1:p.Cys3297Tyr | |
| XM_006724473.2:c.9881G>A | XP_006724536.1:p.Cys3294Tyr | |
| XM_006724474.2:c.10019G>A | XP_006724537.1:p.Cys3340Tyr | |
| XM_006724475.2:c.10019G>A | XP_006724538.1:p.Cys3340Tyr | |
| XM_011545467.1:c.9896G>A | XP_011543769.1:p.Cys3299Tyr | |
| XM_006724469.3:c.9995G>A | XP_006724532.1:p.Cys3332Tyr | |
| XM_006724470.3:c.10019G>A | XP_006724533.1:p.Cys3340Tyr | |
| XM_006724474.3:c.10019G>A | XP_006724537.1:p.Cys3340Tyr | |
| XM_017029328.1:c.10019G>A | XP_016884817.1:p.Cys3340Tyr | |
| XM_017029331.1:c.4193G>A | XP_016884820.1:p.Cys1398Tyr | |
| NM_000109.4:c.9995G>A | NP_000100.3:p.Cys3332Tyr | |
| NM_004006.3:c.10019G>A MANE Select | NP_003997.2:p.Cys3340Tyr | |
| NM_004011.4:c.5996G>A | NP_004002.3:p.Cys1999Tyr | |
| NM_004012.4:c.5987G>A | NP_004003.2:p.Cys1996Tyr | |
| NM_004015.3:c.815G>A | NP_004006.1:p.Cys272Tyr | |
| NM_004016.3:c.815G>A | NP_004007.1:p.Cys272Tyr | |
| NM_004017.3:c.815G>A | NP_004008.1:p.Cys272Tyr | |
| NM_004018.3:c.815G>A | NP_004009.1:p.Cys272Tyr | |
| NM_004019.3:c.815G>A | NP_004010.1:p.Cys272Tyr | |
| NM_004021.3:c.2639G>A | NP_004012.2:p.Cys880Tyr | |
| NM_004023.3:c.2639G>A | NP_004014.2:p.Cys880Tyr | |
| NM_004013.3:c.2639G>A | NP_004004.2:p.Cys880Tyr | |
| NM_004014.3:c.1832G>A | NP_004005.2:p.Cys611Tyr | |
| NM_004020.4:c.2639G>A | NP_004011.3:p.Cys880Tyr | |
| NM_004022.3:c.2639G>A | NP_004013.2:p.Cys880Tyr |