Canonical Allele Identifier: CA381520408
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs1138272

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586108C>G , CM000673.2:g.67586108C>G GRCh38
NC_000011.9:g.67353579C>G , CM000673.1:g.67353579C>G GRCh37
NC_000011.8:g.67110155C>G NCBI36
NG_012075.1:g.7514C>G , LRG_723:g.7514C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.337-281C>G ENSP00000381604.1:n.337-281C>G
ENST00000398606.10:c.341C>G MANE Select ENSP00000381607.3:p.Ala114Gly
ENST00000646888.1:c.*57C>G ENSP00000494477.1:n.*57C>G
ENST00000398603.5:c.337-281C>G ENSP00000381604.1:n.337-281C>G
ENST00000398606.7:c.341C>G ENSP00000381607.3:p.Ala114Gly
ENST00000467591.1:n.452C>G
ENST00000494593.1:n.1136C>G
ENST00000495996.1:c.5C>G ENSP00000484686.1:p.Ala2Gly
ENST00000498765.5:c.404C>G
NM_000852.3:c.341C>G , LRG_723t1:c.341C>G NP_000843.1:p.Ala114Gly
NM_000852.4:c.341C>G MANE Select NP_000843.1:p.Ala114Gly