Canonical Allele Identifier: CA1226125363
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431511G= , CM000663.2:g.229431511G= GRCh38
NC_000001.10:g.229567258G= , CM000663.1:g.229567258G= GRCh37
NC_000001.9:g.227633881G= NCBI36
NG_006672.1:g.7586C= , LRG_429:g.7586C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.1044C= ENSP00000355644.4:p.Arg348=
ENST00000684723.1:c.987C= ENSP00000508084.1:p.Arg329=
ENST00000366683.3:c.753C= ENSP00000355644.3:p.Arg251=
ENST00000366684.7:c.1122C= MANE Select ENSP00000355645.3:p.Arg374=
NM_001100.3:c.1122C= , LRG_429t1:c.1122C= NP_001091.1:p.Arg374=
NM_001100.4:c.1122C= MANE Select NP_001091.1:p.Arg374=