Canonical Allele Identifier: CA1226125690
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432215C= , CM000663.2:g.229432215C= GRCh38
NC_000001.10:g.229567962C= , CM000663.1:g.229567962C= GRCh37
NC_000001.9:g.227634585C= NCBI36
NG_006672.1:g.6882G= , LRG_429:g.6882G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.617-30G= ENSP00000355644.4:n.617-30G=
ENST00000684723.1:c.482-30G= ENSP00000508084.1:n.482-30G=
ENST00000366683.3:c.479+192G= ENSP00000355644.3:n.479+192G=
ENST00000366684.7:c.617-30G= MANE Select ENSP00000355645.3:n.617-30G=
NM_001100.3:c.617-30G= , LRG_429t1:c.617-30G= NP_001091.1:n.617-30G=
NM_001100.4:c.617-30G= MANE Select NP_001091.1:n.617-30G=