Canonical Allele Identifier: CA475395905
Gene: GSTP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.67353583C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586112C>G , CM000673.2:g.67586112C>G GRCh38
NC_000011.9:g.67353583C>G , CM000673.1:g.67353583C>G GRCh37
NC_000011.8:g.67110159C>G NCBI36
NG_012075.1:g.7518C>G , LRG_723:g.7518C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000398603.6:c.337-277C>G ENSP00000381604.1:n.337-277C>G
ENST00000398606.10:c.345C>G MANE Select ENSP00000381607.3:p.Gly115=
ENST00000646888.1:c.*61C>G ENSP00000494477.1:n.*61C>G
ENST00000398603.5:c.337-277C>G ENSP00000381604.1:n.337-277C>G
ENST00000398606.7:c.345C>G ENSP00000381607.3:p.Gly115=
ENST00000467591.1:n.456C>G
ENST00000494593.1:n.1140C>G
ENST00000495996.1:c.9C>G ENSP00000484686.1:p.Gly3=
ENST00000498765.5:c.408C>G
NM_000852.3:c.345C>G , LRG_723t1:c.345C>G NP_000843.1:p.Gly115=
NM_000852.4:c.345C>G MANE Select NP_000843.1:p.Gly115=