Canonical Allele Identifier: CA1226125770
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432409G= , CM000663.2:g.229432409G= GRCh38
NC_000001.10:g.229568156G= , CM000663.1:g.229568156G= GRCh37
NC_000001.9:g.227634779G= NCBI36
NG_006672.1:g.6688C= , LRG_429:g.6688C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.477C= ENSP00000355644.4:p.Asp159=
ENST00000684723.1:c.342C= ENSP00000508084.1:p.Asp114=
ENST00000366683.3:c.477C= ENSP00000355644.3:p.Asp159=
ENST00000366684.7:c.477C= MANE Select ENSP00000355645.3:p.Asp159=
NM_001100.3:c.477C= , LRG_429t1:c.477C= NP_001091.1:p.Asp159=
NM_001100.4:c.477C= MANE Select NP_001091.1:p.Asp159=