Linked Data
dbSNP Id:
rs765676218
ExAC:
17:80882895 G / A
gnomAD v2:
17-80882895-G-A
gnomAD v3:
17-82925019-G-A
gnomAD v4:
17-82925019-G-A
COSMIC:
COSM4070968
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.82925019G>A , CM000679.2:g.82925019G>A | GRCh38 |
| NC_000017.10:g.80882895G>A , CM000679.1:g.80882895G>A | GRCh37 |
| NC_000017.9:g.78476184G>A | NCBI36 |
| NG_011721.1:g.177956G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000574886.2:n.1549G>A | ||
| ENST00000576677.6:n.1470G>A | ||
| ENST00000681983.1:n.2477G>A | ||
| ENST00000682099.1:n.1238G>A | ||
| ENST00000682213.1:c.*312G>A | ENSP00000508166.1:n.*312G>A | |
| ENST00000682315.1:c.655G>A | ENSP00000507232.1:p.Ala219Thr | |
| ENST00000682479.1:c.2431G>A | ENSP00000508214.1:p.Ala811Thr | |
| ENST00000682610.1:n.1581G>A | ||
| ENST00000682654.1:c.*312G>A | ENSP00000507412.1:n.*312G>A | |
| ENST00000682722.1:c.2290G>A | ENSP00000508364.1:p.Ala764Thr | |
| ENST00000683041.1:c.*312G>A | ENSP00000506994.1:n.*312G>A | |
| ENST00000683184.1:c.*1994G>A | ENSP00000507757.1:n.*1994G>A | |
| ENST00000683282.1:c.2257G>A | ENSP00000506913.1:p.Ala753Thr | |
| ENST00000683444.1:c.*1918G>A | ENSP00000507553.1:n.*1918G>A | |
| ENST00000683584.1:n.1164G>A | ||
| ENST00000683821.1:c.655G>A | ENSP00000507651.1:p.Ala219Thr | |
| ENST00000683839.1:n.1795G>A | ||
| ENST00000684000.1:c.2425G>A | ENSP00000506795.1:p.Ala809Thr | |
| ENST00000684188.1:c.2152G>A | ENSP00000507153.1:p.Ala718Thr | |
| ENST00000684349.1:c.2527G>A | ENSP00000508067.1:p.Ala843Thr | |
| ENST00000684361.1:c.2341G>A | ENSP00000507364.1:p.Ala781Thr | |
| ENST00000684408.1:c.1984G>A | ENSP00000506837.1:p.Ala662Thr | |
| ENST00000684429.1:c.2269G>A | ENSP00000507224.1:p.Ala757Thr | |
| ENST00000684464.1:c.2434G>A | ENSP00000508333.1:p.Ala812Thr | |
| ENST00000684544.1:c.2260G>A | ENSP00000507337.1:p.Ala754Thr | |
| ENST00000684559.1:n.1096G>A | ||
| ENST00000684760.1:c.2608G>A | ENSP00000507696.1:p.Ala870Thr | |
| ENST00000684776.1:c.*824G>A | ENSP00000507861.1:n.*824G>A | |
| ENST00000355528.9:c.2341G>A MANE Select | ENSP00000347719.4:p.Ala781Thr | |
| ENST00000355528.8:c.2341G>A | ENSP00000347719.4:p.Ala781Thr | |
| ENST00000539345.6:c.2341G>A | ENSP00000440671.2:p.Ala781Thr | |
| ENST00000571618.5:n.519G>A | ||
| ENST00000571796.5:n.999G>A | ||
| ENST00000574422.1:c.655G>A | ENSP00000458599.1:p.Ala219Thr | |
| ENST00000574818.5:n.399G>A | ||
| ENST00000574886.1:n.725G>A | ||
| ENST00000574975.5:c.718G>A | ENSP00000461680.1:p.Ala240Thr | |
| ENST00000576760.5:c.655G>A | ENSP00000460949.1:p.Ala219Thr | |
| NM_005993.4:c.2341G>A | NP_005984.3:p.Ala781Thr | |
| XM_005256396.3:c.2290G>A | XP_005256453.1:p.Ala764Thr | |
| XM_005256399.3:c.1057G>A | XP_005256456.1:p.Ala353Thr | |
| XM_005256400.3:c.655G>A | XP_005256457.1:p.Ala219Thr | |
| XM_005256401.3:c.655G>A | XP_005256458.1:p.Ala219Thr | |
| XM_005256402.3:c.655G>A | XP_005256459.1:p.Ala219Thr | |
| XM_005256403.3:c.655G>A | XP_005256460.1:p.Ala219Thr | |
| XM_005256404.3:c.655G>A | XP_005256461.1:p.Ala219Thr | |
| XM_006722290.2:c.2260G>A | XP_006722353.1:p.Ala754Thr | |
| XM_006722291.2:c.1045G>A | XP_006722354.1:p.Ala349Thr | |
| XM_006722292.2:c.655G>A | XP_006722355.1:p.Ala219Thr | |
| XM_011523589.1:c.1996G>A | XP_011521891.1:p.Ala666Thr | |
| XM_011523590.1:c.1984G>A | XP_011521892.1:p.Ala662Thr | |
| XM_011523591.1:c.1981G>A | XP_011521893.1:p.Ala661Thr | |
| XM_011523592.1:c.1894G>A | XP_011521894.1:p.Ala632Thr | |
| XM_011523593.1:c.1588G>A | XP_011521895.1:p.Ala530Thr | |
| XM_011523594.1:c.1069G>A | XP_011521896.1:p.Ala357Thr | |
| XM_011523595.1:c.1036G>A | XP_011521897.1:p.Ala346Thr | |
| XM_011523596.1:c.*72G>A | XP_011521898.1:n.*72G>A | |
| XM_011523597.1:c.802G>A | XP_011521899.1:p.Ala268Thr | |
| XM_011523598.1:c.799G>A | XP_011521900.1:p.Ala267Thr | |
| XM_011523599.1:c.793G>A | XP_011521901.1:p.Ala265Thr | |
| XM_011523600.1:c.655G>A | XP_011521902.1:p.Ala219Thr | |
| XR_430033.2:n.2449G>A | ||
| XM_005256396.4:c.2290G>A | XP_005256453.1:p.Ala764Thr | |
| XM_005256399.5:c.1057G>A | XP_005256456.1:p.Ala353Thr | |
| XM_005256404.4:c.655G>A | XP_005256461.1:p.Ala219Thr | |
| XM_006722291.4:c.1045G>A | XP_006722354.1:p.Ala349Thr | |
| XM_006722292.3:c.655G>A | XP_006722355.1:p.Ala219Thr | |
| XM_011523589.2:c.1996G>A | XP_011521891.1:p.Ala666Thr | |
| XM_011523591.2:c.1981G>A | XP_011521893.1:p.Ala661Thr | |
| XM_011523593.2:c.1588G>A | XP_011521895.1:p.Ala530Thr | |
| XM_011523594.2:c.1069G>A | XP_011521896.1:p.Ala357Thr | |
| XM_011523595.3:c.1036G>A | XP_011521897.1:p.Ala346Thr | |
| XM_011523597.2:c.802G>A | XP_011521899.1:p.Ala268Thr | |
| XM_011523599.2:c.793G>A | XP_011521901.1:p.Ala265Thr | |
| XM_011523600.3:c.655G>A | XP_011521902.1:p.Ala219Thr | |
| XM_017024987.1:c.2152G>A | XP_016880476.1:p.Ala718Thr | |
| XM_017024989.1:c.703G>A | XP_016880478.1:p.Ala235Thr | |
| XM_017024990.2:c.655G>A | XP_016880479.1:p.Ala219Thr | |
| XM_024450899.1:c.655G>A | XP_024306667.1:p.Ala219Thr | |
| XM_024450900.1:c.655G>A | XP_024306668.1:p.Ala219Thr | |
| XM_024450901.1:c.655G>A | XP_024306669.1:p.Ala219Thr | |
| XM_024450902.1:c.655G>A | XP_024306670.1:p.Ala219Thr | |
| XR_001752597.1:n.2449G>A | ||
| XR_001752598.1:n.2449G>A | ||
| XR_001752599.1:n.2449G>A | ||
| XR_001752600.1:n.2367G>A | ||
| NM_005993.5:c.2341G>A MANE Select | NP_005984.3:p.Ala781Thr |