Canonical Allele Identifier: CA1226125892
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432605G= , CM000663.2:g.229432605G= GRCh38
NC_000001.10:g.229568352G= , CM000663.1:g.229568352G= GRCh37
NC_000001.9:g.227634975G= NCBI36
NG_006672.1:g.6492C= , LRG_429:g.6492C=

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.405C= ENSP00000355644.4:p.Tyr135=
ENST00000684723.1:c.270C= ENSP00000508084.1:p.Tyr90=
ENST00000366683.3:c.405C= ENSP00000355644.3:p.Tyr135=
ENST00000366684.7:c.405C= MANE Select ENSP00000355645.3:p.Tyr135=
NM_001100.3:c.405C= , LRG_429t1:c.405C= NP_001091.1:p.Tyr135=
NM_001100.4:c.405C= MANE Select NP_001091.1:p.Tyr135=