Canonical Allele Identifier: CA1226125573
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1659947760

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431939G>T , CM000663.2:g.229431939G>T GRCh38
NC_000001.10:g.229567686G>T , CM000663.1:g.229567686G>T GRCh37
NC_000001.9:g.227634309G>T NCBI36
NG_006672.1:g.7158C>A , LRG_429:g.7158C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.809-37C>A ENSP00000355644.4:n.809-37C>A
ENST00000684723.1:c.674-37C>A ENSP00000508084.1:n.674-37C>A
ENST00000366683.3:c.480-77C>A ENSP00000355644.3:n.480-77C>A
ENST00000366684.7:c.809-37C>A MANE Select ENSP00000355645.3:n.809-37C>A
NM_001100.3:c.809-37C>A , LRG_429t1:c.809-37C>A NP_001091.1:n.809-37C>A
NM_001100.4:c.809-37C>A MANE Select NP_001091.1:n.809-37C>A