Canonical Allele Identifier: CA1226125315
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1659930701

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431440G>T , CM000663.2:g.229431440G>T GRCh38
NC_000001.10:g.229567187G>T , CM000663.1:g.229567187G>T GRCh37
NC_000001.9:g.227633810G>T NCBI36
NG_006672.1:g.7657C>A , LRG_429:g.7657C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.*59C>A ENSP00000355644.4:n.*59C>A
ENST00000684723.1:c.*59C>A ENSP00000508084.1:n.*59C>A
ENST00000366683.3:c.*59C>A ENSP00000355644.3:n.*59C>A
ENST00000366684.7:c.*59C>A MANE Select ENSP00000355645.3:n.*59C>A
NM_001100.3:c.*59C>A , LRG_429t1:c.*59C>A NP_001091.1:n.*59C>A
NM_001100.4:c.*59C>A MANE Select NP_001091.1:n.*59C>A