Canonical Allele Identifier: CA1226125723
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432280G= , CM000663.2:g.229432280G= GRCh38
NC_000001.10:g.229568027G= , CM000663.1:g.229568027G= GRCh37
NC_000001.9:g.227634650G= NCBI36
NG_006672.1:g.6817C= , LRG_429:g.6817C=

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.606C= ENSP00000355644.4:p.Phe202=
ENST00000684723.1:c.471C= ENSP00000508084.1:p.Phe157=
ENST00000366683.3:c.479+127C= ENSP00000355644.3:n.479+127C=
ENST00000366684.7:c.606C= MANE Select ENSP00000355645.3:p.Phe202=
NM_001100.3:c.606C= , LRG_429t1:c.606C= NP_001091.1:p.Phe202=
NM_001100.4:c.606C= MANE Select NP_001091.1:p.Phe202=