Canonical Allele Identifier: CA1226125425
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431654C= , CM000663.2:g.229431654C= GRCh38
NC_000001.10:g.229567401C= , CM000663.1:g.229567401C= GRCh37
NC_000001.9:g.227634024C= NCBI36
NG_006672.1:g.7443G= , LRG_429:g.7443G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.990+67G= ENSP00000355644.4:n.990+67G=
ENST00000684723.1:c.856-12G= ENSP00000508084.1:n.856-12G=
ENST00000366683.3:c.622-12G= ENSP00000355644.3:n.622-12G=
ENST00000366684.7:c.991-12G= MANE Select ENSP00000355645.3:n.991-12G=
NM_001100.3:c.991-12G= , LRG_429t1:c.991-12G= NP_001091.1:n.991-12G=
NM_001100.4:c.991-12G= MANE Select NP_001091.1:n.991-12G=