Canonical Allele Identifier: CA1226125377
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431550C= , CM000663.2:g.229431550C= GRCh38
NC_000001.10:g.229567297C= , CM000663.1:g.229567297C= GRCh37
NC_000001.9:g.227633920C= NCBI36
NG_006672.1:g.7547G= , LRG_429:g.7547G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.1005G= ENSP00000355644.4:p.Lys335=
ENST00000684723.1:c.948G= ENSP00000508084.1:p.Lys316=
ENST00000366683.3:c.714G= ENSP00000355644.3:p.Lys238=
ENST00000366684.7:c.1083G= MANE Select ENSP00000355645.3:p.Lys361=
NM_001100.3:c.1083G= , LRG_429t1:c.1083G= NP_001091.1:p.Lys361=
NM_001100.4:c.1083G= MANE Select NP_001091.1:p.Lys361=