Canonical Allele Identifier: CA1226125754
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432358G= , CM000663.2:g.229432358G= GRCh38
NC_000001.10:g.229568105G= , CM000663.1:g.229568105G= GRCh37
NC_000001.9:g.227634728G= NCBI36
NG_006672.1:g.6739C= , LRG_429:g.6739C=

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.528C= ENSP00000355644.4:p.Ala176=
ENST00000684723.1:c.393C= ENSP00000508084.1:p.Ala131=
ENST00000366683.3:c.479+49C= ENSP00000355644.3:n.479+49C=
ENST00000366684.7:c.528C= MANE Select ENSP00000355645.3:p.Ala176=
NM_001100.3:c.528C= , LRG_429t1:c.528C= NP_001091.1:p.Ala176=
NM_001100.4:c.528C= MANE Select NP_001091.1:p.Ala176=