Canonical Allele Identifier: CA1226125536
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431902C= , CM000663.2:g.229431902C= GRCh38
NC_000001.10:g.229567649C= , CM000663.1:g.229567649C= GRCh37
NC_000001.9:g.227634272C= NCBI36
NG_006672.1:g.7195G= , LRG_429:g.7195G=

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.809G= ENSP00000355644.4:p.Gly270=
ENST00000684723.1:c.674G= ENSP00000508084.1:p.Gly225=
ENST00000366683.3:c.480-40G= ENSP00000355644.3:n.480-40G=
ENST00000366684.7:c.809G= MANE Select ENSP00000355645.3:p.Gly270=
NM_001100.3:c.809G= , LRG_429t1:c.809G= NP_001091.1:p.Gly270=
NM_001100.4:c.809G= MANE Select NP_001091.1:p.Gly270=