Canonical Allele Identifier: CA1226125748
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432334G= , CM000663.2:g.229432334G= GRCh38
NC_000001.10:g.229568081G= , CM000663.1:g.229568081G= GRCh37
NC_000001.9:g.227634704G= NCBI36
NG_006672.1:g.6763C= , LRG_429:g.6763C=

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.552C= ENSP00000355644.4:p.Gly184=
ENST00000684723.1:c.417C= ENSP00000508084.1:p.Gly139=
ENST00000366683.3:c.479+73C= ENSP00000355644.3:n.479+73C=
ENST00000366684.7:c.552C= MANE Select ENSP00000355645.3:p.Gly184=
NM_001100.3:c.552C= , LRG_429t1:c.552C= NP_001091.1:p.Gly184=
NM_001100.4:c.552C= MANE Select NP_001091.1:p.Gly184=