Canonical Allele Identifier: CA475396044
Gene: GSTP1 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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