Canonical Allele Identifier: CA1442758
Gene: ACTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1154282
ClinVar RCV Id: RCV001496208
dbSNP Id: rs746042348

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431829G>A , CM000663.2:g.229431829G>A GRCh38
NC_000001.10:g.229567576G>A , CM000663.1:g.229567576G>A GRCh37
NC_000001.9:g.227634199G>A NCBI36
NG_006672.1:g.7268C>T , LRG_429:g.7268C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.882C>T ENSP00000355644.4:p.Asp294=
ENST00000684723.1:c.747C>T ENSP00000508084.1:p.Asp249=
ENST00000366683.3:c.513C>T ENSP00000355644.3:p.Asp171=
ENST00000366684.7:c.882C>T MANE Select ENSP00000355645.3:p.Asp294=
NM_001100.3:c.882C>T , LRG_429t1:c.882C>T NP_001091.1:p.Asp294=
NM_001100.4:c.882C>T MANE Select NP_001091.1:p.Asp294=