Canonical Allele Identifier: CA475396043
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67353643C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586172C>A , CM000673.2:g.67586172C>A GRCh38
NC_000011.9:g.67353643C>A , CM000673.1:g.67353643C>A GRCh37
NC_000011.8:g.67110219C>A NCBI36
NG_012075.1:g.7578C>A , LRG_723:g.7578C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-217C>A ENSP00000381604.1:n.337-217C>A
ENST00000398606.10:c.405C>A MANE Select ENSP00000381607.3:p.Ser135=
ENST00000646888.1:c.*121C>A ENSP00000494477.1:n.*121C>A
ENST00000398603.5:c.337-217C>A ENSP00000381604.1:n.337-217C>A
ENST00000398606.7:c.405C>A ENSP00000381607.3:p.Ser135=
ENST00000467591.1:n.516C>A
ENST00000494593.1:n.1200C>A
ENST00000495996.1:c.69C>A ENSP00000484686.1:p.Ser23=
ENST00000498765.5:c.468C>A
NM_000852.3:c.405C>A , LRG_723t1:c.405C>A NP_000843.1:p.Ser135=
NM_000852.4:c.405C>A MANE Select NP_000843.1:p.Ser135=