Canonical Allele Identifier: CA1226125681
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432203A= , CM000663.2:g.229432203A= GRCh38
NC_000001.10:g.229567950A= , CM000663.1:g.229567950A= GRCh37
NC_000001.9:g.227634573A= NCBI36
NG_006672.1:g.6894T= , LRG_429:g.6894T=

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.617-18T= ENSP00000355644.4:n.617-18T=
ENST00000684723.1:c.482-18T= ENSP00000508084.1:n.482-18T=
ENST00000366683.3:c.479+204T= ENSP00000355644.3:n.479+204T=
ENST00000366684.7:c.617-18T= MANE Select ENSP00000355645.3:n.617-18T=
NM_001100.3:c.617-18T= , LRG_429t1:c.617-18T= NP_001091.1:n.617-18T=
NM_001100.4:c.617-18T= MANE Select NP_001091.1:n.617-18T=