Canonical Allele Identifier: CA1226125728
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432294G= , CM000663.2:g.229432294G= GRCh38
NC_000001.10:g.229568041G= , CM000663.1:g.229568041G= GRCh37
NC_000001.9:g.227634664G= NCBI36
NG_006672.1:g.6803C= , LRG_429:g.6803C=

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.592C= ENSP00000355644.4:p.Arg198=
ENST00000684723.1:c.457C= ENSP00000508084.1:p.Arg153=
ENST00000366683.3:c.479+113C= ENSP00000355644.3:n.479+113C=
ENST00000366684.7:c.592C= MANE Select ENSP00000355645.3:p.Arg198=
NM_001100.3:c.592C= , LRG_429t1:c.592C= NP_001091.1:p.Arg198=
NM_001100.4:c.592C= MANE Select NP_001091.1:p.Arg198=