Linked Data
ClinVar Variation Id:
43180
ClinVar RCV Id:
RCV000036084
RCV000270954
RCV000383860
RCV000326027
RCV004018785
RCV000727020
RCV001276689
dbSNP Id:
rs201203036
ExAC:
11:76890101 C / A
gnomAD v2:
11-76890101-C-A
gnomAD v3:
11-77179055-C-A
gnomAD v4:
11-77179055-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.77179055C>A , CM000673.2:g.77179055C>A | GRCh38 |
| NC_000011.9:g.76890101C>A , CM000673.1:g.76890101C>A | GRCh37 |
| NC_000011.8:g.76567749C>A | NCBI36 |
| NG_009086.1:g.55792C>A | |
| NG_009086.2:g.55810C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409709.9:c.2293C>A MANE Select | ENSP00000386331.3:p.Leu765Met | |
| ENST00000409893.6:c.358C>A | ENSP00000386689.2:p.Leu120Met | |
| ENST00000670577.1:c.134C>A | ||
| ENST00000409619.6:c.2260C>A | ENSP00000386635.2:p.Leu754Met | |
| ENST00000409709.7:c.2293C>A | ENSP00000386331.3:p.Leu765Met | |
| ENST00000409893.5:c.2293C>A | ENSP00000386689.1:p.Leu765Met | |
| ENST00000458637.6:c.2293C>A | ENSP00000392185.2:p.Leu765Met | |
| ENST00000620575.4:c.2293C>A | ENSP00000477640.1:p.Leu765Met | |
| NM_000260.3:c.2293C>A | NP_000251.3:p.Leu765Met | |
| NM_001127179.2:c.2293C>A | NP_001120651.2:p.Leu765Met | |
| NM_001127180.1:c.2293C>A | NP_001120652.1:p.Leu765Met | |
| XM_005274012.2:c.2293C>A | XP_005274069.1:p.Leu765Met | |
| XM_006718558.2:c.2293C>A | XP_006718621.1:p.Leu765Met | |
| XM_006718559.2:c.2293C>A | XP_006718622.1:p.Leu765Met | |
| XM_006718560.2:c.2293C>A | XP_006718623.1:p.Leu765Met | |
| XM_006718561.2:c.2293C>A | XP_006718624.1:p.Leu765Met | |
| XM_011545044.1:c.2293C>A | XP_011543346.1:p.Leu765Met | |
| XM_011545045.1:c.2293C>A | XP_011543347.1:p.Leu765Met | |
| XM_011545046.1:c.2260C>A | XP_011543348.1:p.Leu754Met | |
| XM_011545047.1:c.2293C>A | XP_011543349.1:p.Leu765Met | |
| XM_011545048.1:c.2293C>A | XP_011543350.1:p.Leu765Met | |
| XM_011545049.1:c.2062C>A | XP_011543351.1:p.Leu688Met | |
| XM_011545050.1:c.2035C>A | XP_011543352.1:p.Leu679Met | |
| XM_011545051.1:c.2293C>A | XP_011543353.1:p.Leu765Met | |
| XM_011545052.1:c.2293C>A | XP_011543354.1:p.Leu765Met | |
| XR_949938.1:n.2613C>A | ||
| XR_949941.1:n.2613C>A | ||
| XR_949942.1:n.2615C>A | ||
| XR_949943.1:n.2615C>A | ||
| XM_011545044.2:c.2293C>A | XP_011543346.1:p.Leu765Met | |
| XM_011545046.2:c.2383C>A | XP_011543348.2:p.Leu795Met | |
| XM_011545050.2:c.2035C>A | XP_011543352.1:p.Leu679Met | |
| XM_017017778.1:c.2383C>A | XP_016873267.1:p.Leu795Met | |
| XM_017017779.1:c.2383C>A | XP_016873268.1:p.Leu795Met | |
| XM_017017780.1:c.2383C>A | XP_016873269.1:p.Leu795Met | |
| XM_017017781.1:c.2383C>A | XP_016873270.1:p.Leu795Met | |
| XM_017017782.1:c.2383C>A | XP_016873271.1:p.Leu795Met | |
| XM_017017783.1:c.2383C>A | XP_016873272.1:p.Leu795Met | |
| XM_017017784.1:c.2383C>A | XP_016873273.1:p.Leu795Met | |
| XM_017017785.1:c.2152C>A | XP_016873274.1:p.Leu718Met | |
| XM_017017786.1:c.2383C>A | XP_016873275.1:p.Leu795Met | |
| XM_017017787.1:c.2383C>A | XP_016873276.1:p.Leu795Met | |
| XM_017017788.1:c.2383C>A | XP_016873277.1:p.Leu795Met | |
| XR_001747885.1:n.2398C>A | ||
| XR_001747886.1:n.2398C>A | ||
| XR_001747887.1:n.2398C>A | ||
| XR_001747888.1:n.2398C>A | ||
| XR_001747889.1:n.2398C>A | ||
| NM_000260.4:c.2293C>A MANE Select | NP_000251.3:p.Leu765Met | |
| NM_001127180.2:c.2293C>A | NP_001120652.1:p.Leu765Met | |
| NM_001369365.1:c.2260C>A | NP_001356294.1:p.Leu754Met |