Canonical Allele Identifier: CA1226125952
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432756T= , CM000663.2:g.229432756T= GRCh38
NC_000001.10:g.229568503T= , CM000663.1:g.229568503T= GRCh37
NC_000001.9:g.227635126T= NCBI36
NG_006672.1:g.6341A= , LRG_429:g.6341A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.254A= ENSP00000355644.4:p.Glu85=
ENST00000684723.1:c.119A= ENSP00000508084.1:p.Glu40=
ENST00000366683.3:c.254A= ENSP00000355644.3:p.Glu85=
ENST00000366684.7:c.254A= MANE Select ENSP00000355645.3:p.Glu85=
NM_001100.3:c.254A= , LRG_429t1:c.254A= NP_001091.1:p.Glu85=
NM_001100.4:c.254A= MANE Select NP_001091.1:p.Glu85=