Canonical Allele Identifier: CA1226125727
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432292A= , CM000663.2:g.229432292A= GRCh38
NC_000001.10:g.229568039A= , CM000663.1:g.229568039A= GRCh37
NC_000001.9:g.227634662A= NCBI36
NG_006672.1:g.6805T= , LRG_429:g.6805T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.594T= ENSP00000355644.4:p.Arg198=
ENST00000684723.1:c.459T= ENSP00000508084.1:p.Arg153=
ENST00000366683.3:c.479+115T= ENSP00000355644.3:n.479+115T=
ENST00000366684.7:c.594T= MANE Select ENSP00000355645.3:p.Arg198=
NM_001100.3:c.594T= , LRG_429t1:c.594T= NP_001091.1:p.Arg198=
NM_001100.4:c.594T= MANE Select NP_001091.1:p.Arg198=