Linked Data
ClinVar Variation Id:
11823
ClinVar RCV Id:
RCV000012596
RCV000020628
RCV000224266
RCV000414791
RCV000544176
RCV001004016
RCV001374894
RCV001197458
RCV001257756
RCV001249626
RCV002326676
RCV002466399
dbSNP Id:
rs28934908
gnomAD v4:
X-154031409-G-A
COSMIC:
COSM1466731
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154031409G>A , CM000685.2:g.154031409G>A | GRCh38 |
| NC_000023.10:g.153296860G>A , CM000685.1:g.153296860G>A | GRCh37 |
| NC_000023.9:g.152950054G>A | NCBI36 |
| NG_007107.2:g.110719C>T | |
| NG_007107.3:g.110695C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303391.11:c.419C>T MANE Plus Clinical | ENSP00000301948.6:p.Ala140Val | |
| ENST00000453960.7:c.455C>T MANE Select | ENSP00000395535.2:p.Ala152Val | |
| ENST00000637917.1:c.52C>T | ||
| ENST00000303391.10:c.419C>T | ENSP00000301948.6:p.Ala140Val | |
| ENST00000369957.5:c.*473C>T | ENSP00000358973.4:n.*473C>T | |
| ENST00000407218.5:c.455C>T | ENSP00000384865.2:p.Ala152Val | |
| ENST00000453960.6:c.455C>T | ENSP00000395535.2:p.Ala152Val | |
| ENST00000486506.5:n.2767C>T | ||
| ENST00000611468.1:c.407C>T | ENSP00000479736.1:p.Ala136Val | |
| ENST00000619732.4:c.419C>T | ENSP00000480973.1:p.Ala140Val | |
| ENST00000622433.4:c.407C>T | ENSP00000484470.1:p.Ala136Val | |
| ENST00000628176.2:c.419C>T | ENSP00000486978.1:p.Ala140Val | |
| NM_001110792.1:c.455C>T | NP_001104262.1:p.Ala152Val | |
| NM_001316337.1:c.140C>T | NP_001303266.1:p.Ala47Val | |
| NM_004992.3:c.419C>T | NP_004983.1:p.Ala140Val | |
| XM_005274681.3:c.419C>T | XP_005274738.1:p.Ala140Val | |
| XM_005274682.3:c.140C>T | XP_005274739.1:p.Ala47Val | |
| XM_005274683.3:c.140C>T | XP_005274740.1:p.Ala47Val | |
| XM_006724819.2:c.-142C>T | XP_006724882.1:n.-142C>T | |
| XM_011531166.1:c.140C>T | XP_011529468.1:p.Ala47Val | |
| XM_006724819.3:c.-142C>T | XP_006724882.1:n.-142C>T | |
| XM_011531166.2:c.140C>T | XP_011529468.1:p.Ala47Val | |
| XM_024452383.1:c.140C>T | XP_024308151.1:p.Ala47Val | |
| XM_024452384.1:c.140C>T | XP_024308152.1:p.Ala47Val | |
| NM_001110792.2:c.455C>T MANE Select | NP_001104262.1:p.Ala152Val | |
| NM_001316337.2:c.140C>T | NP_001303266.1:p.Ala47Val | |
| NM_001369391.2:c.140C>T | NP_001356320.1:p.Ala47Val | |
| NM_001369392.2:c.140C>T | NP_001356321.1:p.Ala47Val | |
| NM_001369393.2:c.140C>T | NP_001356322.1:p.Ala47Val | |
| NM_001369394.1:c.140C>T | NP_001356323.1:p.Ala47Val | |
| NM_001369394.2:c.140C>T | NP_001356323.1:p.Ala47Val | |
| NM_001386137.1:c.-142C>T | NP_001373066.1:n.-142C>T | |
| NM_001386138.1:c.-142C>T | NP_001373067.1:n.-142C>T | |
| NM_001386139.1:c.-142C>T | NP_001373068.1:n.-142C>T | |
| NM_004992.4:c.419C>T MANE Plus Clinical | NP_004983.1:p.Ala140Val |