Canonical Allele Identifier: CA1226125379
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431555T= , CM000663.2:g.229431555T= GRCh38
NC_000001.10:g.229567302T= , CM000663.1:g.229567302T= GRCh37
NC_000001.9:g.227633925T= NCBI36
NG_006672.1:g.7542A= , LRG_429:g.7542A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.1000A= ENSP00000355644.4:p.Thr334=
ENST00000684723.1:c.943A= ENSP00000508084.1:p.Thr315=
ENST00000366683.3:c.709A= ENSP00000355644.3:p.Thr237=
ENST00000366684.7:c.1078A= MANE Select ENSP00000355645.3:p.Thr360=
NM_001100.3:c.1078A= , LRG_429t1:c.1078A= NP_001091.1:p.Thr360=
NM_001100.4:c.1078A= MANE Select NP_001091.1:p.Thr360=