Canonical Allele Identifier: CA6142838

Gene: GSTP1

Linked Data

• dbSNP Id: rs71534227
• ExAC: 11:67353654 G / A
• gnomAD v2: 11-67353654-G-A
• gnomAD v3: 11-67586183-G-A
• gnomAD v4: 11-67586183-G-A
• MyVariant Identifiers: chr11:g.67353654G>A (hg19) ; chr11:g.67586183G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586183G>A , CM000673.2:g.67586183G>A	GRCh38
NC_000011.9:g.67353654G>A , CM000673.1:g.67353654G>A	GRCh37
NC_000011.8:g.67110230G>A	NCBI36
NG_012075.1:g.7589G>A , LRG_723:g.7589G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.337-206G>A	ENSP00000381604.1:n.337-206G>A
ENST00000398606.10:c.416G>A MANE Select	ENSP00000381607.3:p.Gly139Glu
ENST00000646888.1:c.*132G>A	ENSP00000494477.1:n.*132G>A
ENST00000398603.5:c.337-206G>A	ENSP00000381604.1:n.337-206G>A
ENST00000398606.7:c.416G>A	ENSP00000381607.3:p.Gly139Glu
ENST00000467591.1:n.527G>A
ENST00000494593.1:n.1211G>A
ENST00000495996.1:c.80G>A	ENSP00000484686.1:p.Gly27Glu
ENST00000498765.5:c.479G>A
NM_000852.3:c.416G>A , LRG_723t1:c.416G>A	NP_000843.1:p.Gly139Glu
NM_000852.4:c.416G>A MANE Select	NP_000843.1:p.Gly139Glu