Canonical Allele Identifier: CA1226125658
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432135G= , CM000663.2:g.229432135G= GRCh38
NC_000001.10:g.229567882G= , CM000663.1:g.229567882G= GRCh37
NC_000001.9:g.227634505G= NCBI36
NG_006672.1:g.6962C= , LRG_429:g.6962C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.667C= ENSP00000355644.4:p.Leu223=
ENST00000684723.1:c.532C= ENSP00000508084.1:p.Leu178=
ENST00000366683.3:c.480-273C= ENSP00000355644.3:n.480-273C=
ENST00000366684.7:c.667C= MANE Select ENSP00000355645.3:p.Leu223=
NM_001100.3:c.667C= , LRG_429t1:c.667C= NP_001091.1:p.Leu223=
NM_001100.4:c.667C= MANE Select NP_001091.1:p.Leu223=