Canonical Allele Identifier: CA1226125665
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432159T= , CM000663.2:g.229432159T= GRCh38
NC_000001.10:g.229567906T= , CM000663.1:g.229567906T= GRCh37
NC_000001.9:g.227634529T= NCBI36
NG_006672.1:g.6938A= , LRG_429:g.6938A=

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.643A= ENSP00000355644.4:p.Lys215=
ENST00000684723.1:c.508A= ENSP00000508084.1:p.Lys170=
ENST00000366683.3:c.479+248A= ENSP00000355644.3:n.479+248A=
ENST00000366684.7:c.643A= MANE Select ENSP00000355645.3:p.Lys215=
NM_001100.3:c.643A= , LRG_429t1:c.643A= NP_001091.1:p.Lys215=
NM_001100.4:c.643A= MANE Select NP_001091.1:p.Lys215=