Canonical Allele Identifier: CA1226125803
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432470G= , CM000663.2:g.229432470G= GRCh38
NC_000001.10:g.229568217G= , CM000663.1:g.229568217G= GRCh37
NC_000001.9:g.227634840G= NCBI36
NG_006672.1:g.6627C= , LRG_429:g.6627C=

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.455-39C= ENSP00000355644.4:n.455-39C=
ENST00000684723.1:c.320-39C= ENSP00000508084.1:n.320-39C=
ENST00000366683.3:c.455-39C= ENSP00000355644.3:n.455-39C=
ENST00000366684.7:c.455-39C= MANE Select ENSP00000355645.3:n.455-39C=
NM_001100.3:c.455-39C= , LRG_429t1:c.455-39C= NP_001091.1:n.455-39C=
NM_001100.4:c.455-39C= MANE Select NP_001091.1:n.455-39C=