Canonical Allele Identifier: CA423755345
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1659961919
MyVariant Identifiers: chr1:g.229568036G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432289G>T , CM000663.2:g.229432289G>T GRCh38
NC_000001.10:g.229568036G>T , CM000663.1:g.229568036G>T GRCh37
NC_000001.9:g.227634659G>T NCBI36
NG_006672.1:g.6808C>A , LRG_429:g.6808C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.597C>A ENSP00000355644.4:p.Gly199=
ENST00000684723.1:c.462C>A ENSP00000508084.1:p.Gly154=
ENST00000366683.3:c.479+118C>A ENSP00000355644.3:n.479+118C>A
ENST00000366684.7:c.597C>A MANE Select ENSP00000355645.3:p.Gly199=
NM_001100.3:c.597C>A , LRG_429t1:c.597C>A NP_001091.1:p.Gly199=
NM_001100.4:c.597C>A MANE Select NP_001091.1:p.Gly199=