Canonical Allele Identifier: CA1226125431
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431663T= , CM000663.2:g.229431663T= GRCh38
NC_000001.10:g.229567410T= , CM000663.1:g.229567410T= GRCh37
NC_000001.9:g.227634033T= NCBI36
NG_006672.1:g.7434A= , LRG_429:g.7434A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.990+58A= ENSP00000355644.4:n.990+58A=
ENST00000684723.1:c.856-21A= ENSP00000508084.1:n.856-21A=
ENST00000366683.3:c.622-21A= ENSP00000355644.3:n.622-21A=
ENST00000366684.7:c.991-21A= MANE Select ENSP00000355645.3:n.991-21A=
NM_001100.3:c.991-21A= , LRG_429t1:c.991-21A= NP_001091.1:n.991-21A=
NM_001100.4:c.991-21A= MANE Select NP_001091.1:n.991-21A=