Canonical Allele Identifier: CA1226125802
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432468G= , CM000663.2:g.229432468G= GRCh38
NC_000001.10:g.229568215G= , CM000663.1:g.229568215G= GRCh37
NC_000001.9:g.227634838G= NCBI36
NG_006672.1:g.6629C= , LRG_429:g.6629C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.455-37C= ENSP00000355644.4:n.455-37C=
ENST00000684723.1:c.320-37C= ENSP00000508084.1:n.320-37C=
ENST00000366683.3:c.455-37C= ENSP00000355644.3:n.455-37C=
ENST00000366684.7:c.455-37C= MANE Select ENSP00000355645.3:n.455-37C=
NM_001100.3:c.455-37C= , LRG_429t1:c.455-37C= NP_001091.1:n.455-37C=
NM_001100.4:c.455-37C= MANE Select NP_001091.1:n.455-37C=