Canonical Allele Identifier: CA1226125792
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432451A= , CM000663.2:g.229432451A= GRCh38
NC_000001.10:g.229568198A= , CM000663.1:g.229568198A= GRCh37
NC_000001.9:g.227634821A= NCBI36
NG_006672.1:g.6646T= , LRG_429:g.6646T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.455-20T= ENSP00000355644.4:n.455-20T=
ENST00000684723.1:c.320-20T= ENSP00000508084.1:n.320-20T=
ENST00000366683.3:c.455-20T= ENSP00000355644.3:n.455-20T=
ENST00000366684.7:c.455-20T= MANE Select ENSP00000355645.3:n.455-20T=
NM_001100.3:c.455-20T= , LRG_429t1:c.455-20T= NP_001091.1:n.455-20T=
NM_001100.4:c.455-20T= MANE Select NP_001091.1:n.455-20T=