Canonical Allele Identifier: CA1226125366
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431521A= , CM000663.2:g.229431521A= GRCh38
NC_000001.10:g.229567268A= , CM000663.1:g.229567268A= GRCh37
NC_000001.9:g.227633891A= NCBI36
NG_006672.1:g.7576T= , LRG_429:g.7576T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.1034T= ENSP00000355644.4:p.Ile345=
ENST00000684723.1:c.977T= ENSP00000508084.1:p.Ile326=
ENST00000366683.3:c.743T= ENSP00000355644.3:p.Ile248=
ENST00000366684.7:c.1112T= MANE Select ENSP00000355645.3:p.Ile371=
NM_001100.3:c.1112T= , LRG_429t1:c.1112T= NP_001091.1:p.Ile371=
NM_001100.4:c.1112T= MANE Select NP_001091.1:p.Ile371=