Canonical Allele Identifier: CA1143538617
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432181C= , CM000663.2:g.229432181C= GRCh38
NC_000001.10:g.229567928C= , CM000663.1:g.229567928C= GRCh37
NC_000001.9:g.227634551C= NCBI36
NG_006672.1:g.6916G= , LRG_429:g.6916G=

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.621G= ENSP00000355644.4:p.Glu207=
ENST00000684723.1:c.486G= ENSP00000508084.1:p.Glu162=
ENST00000366683.3:c.479+226G= ENSP00000355644.3:n.479+226G=
ENST00000366684.7:c.621G= MANE Select ENSP00000355645.3:p.Glu207=
NM_001100.3:c.621G= , LRG_429t1:c.621G= NP_001091.1:p.Glu207=
NM_001100.4:c.621G= MANE Select NP_001091.1:p.Glu207=