Canonical Allele Identifier: CA1226125659
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432141C= , CM000663.2:g.229432141C= GRCh38
NC_000001.10:g.229567888C= , CM000663.1:g.229567888C= GRCh37
NC_000001.9:g.227634511C= NCBI36
NG_006672.1:g.6956G= , LRG_429:g.6956G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.661G= ENSP00000355644.4:p.Val221=
ENST00000684723.1:c.526G= ENSP00000508084.1:p.Val176=
ENST00000366683.3:c.479+266G= ENSP00000355644.3:n.479+266G=
ENST00000366684.7:c.661G= MANE Select ENSP00000355645.3:p.Val221=
NM_001100.3:c.661G= , LRG_429t1:c.661G= NP_001091.1:p.Val221=
NM_001100.4:c.661G= MANE Select NP_001091.1:p.Val221=