Linked Data
ClinVar Variation Id:
143491
ClinVar RCV Id:
RCV000133022
dbSNP Id:
rs61754432
PubMed:
PMID:11214906
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154032438G>T , CM000685.2:g.154032438G>T | GRCh38 |
| NC_000023.10:g.153297889G>T , CM000685.1:g.153297889G>T | GRCh37 |
| NC_000023.9:g.152951083G>T | NCBI36 |
| NG_007107.2:g.109690C>A | |
| NG_007107.3:g.109666C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303391.11:c.146C>A MANE Plus Clinical | ENSP00000301948.6:p.Ser49Ter | |
| ENST00000453960.7:c.182C>A MANE Select | ENSP00000395535.2:p.Ser61Ter | |
| ENST00000303391.10:c.146C>A | ENSP00000301948.6:p.Ser49Ter | |
| ENST00000369957.5:c.*200C>A | ENSP00000358973.4:n.*200C>A | |
| ENST00000407218.5:c.182C>A | ENSP00000384865.2:p.Ser61Ter | |
| ENST00000415944.3:c.146C>A | ENSP00000416267.1:p.Ser49Ter | |
| ENST00000453960.6:c.182C>A | ENSP00000395535.2:p.Ser61Ter | |
| ENST00000460227.4:n.1295C>A | ||
| ENST00000463644.5:n.1085C>A | ||
| ENST00000481807.3:n.432C>A | ||
| ENST00000486506.5:n.2494C>A | ||
| ENST00000488293.4:n.1195C>A | ||
| ENST00000496908.5:n.277C>A | ||
| ENST00000611468.1:c.134C>A | ENSP00000479736.1:p.Ser45Ter | |
| ENST00000619732.4:c.146C>A | ENSP00000480973.1:p.Ser49Ter | |
| ENST00000622433.4:c.134C>A | ENSP00000484470.1:p.Ser45Ter | |
| ENST00000628176.2:c.146C>A | ENSP00000486978.1:p.Ser49Ter | |
| ENST00000631210.1:n.425C>A | ||
| NM_001110792.1:c.182C>A | NP_001104262.1:p.Ser61Ter | |
| NM_001316337.1:c.-134C>A | NP_001303266.1:n.-134C>A | |
| NM_004992.3:c.146C>A | NP_004983.1:p.Ser49Ter | |
| XM_005274681.3:c.146C>A | XP_005274738.1:p.Ser49Ter | |
| XM_005274682.3:c.-134C>A | XP_005274739.1:n.-134C>A | |
| XM_005274683.3:c.-134C>A | XP_005274740.1:n.-134C>A | |
| XM_011531166.1:c.-134C>A | XP_011529468.1:n.-134C>A | |
| XM_006724819.3:c.-415C>A | XP_006724882.1:n.-415C>A | |
| XM_011531166.2:c.-134C>A | XP_011529468.1:n.-134C>A | |
| XM_024452383.1:c.-134C>A | XP_024308151.1:n.-134C>A | |
| XM_024452384.1:c.-134C>A | XP_024308152.1:n.-134C>A | |
| NM_001110792.2:c.182C>A MANE Select | NP_001104262.1:p.Ser61Ter | |
| NM_001316337.2:c.-134C>A | NP_001303266.1:n.-134C>A | |
| NM_001369391.2:c.-134C>A | NP_001356320.1:n.-134C>A | |
| NM_001369392.2:c.-134C>A | NP_001356321.1:n.-134C>A | |
| NM_001369393.2:c.-134C>A | NP_001356322.1:n.-134C>A | |
| NM_001369394.1:c.-134C>A | NP_001356323.1:n.-134C>A | |
| NM_001369394.2:c.-134C>A | NP_001356323.1:n.-134C>A | |
| NM_001386137.1:c.-415C>A | NP_001373066.1:n.-415C>A | |
| NM_001386138.1:c.-415C>A | NP_001373067.1:n.-415C>A | |
| NM_001386139.1:c.-415C>A | NP_001373068.1:n.-415C>A | |
| NM_004992.4:c.146C>A MANE Plus Clinical | NP_004983.1:p.Ser49Ter |