Canonical Allele Identifier: CA6142843

Gene: GSTP1

Linked Data

• dbSNP Id: rs774028206
• ExAC: 11:67353673 G / A
• gnomAD v2: 11-67353673-G-A
• gnomAD v3: 11-67586202-G-A
• gnomAD v4: 11-67586202-G-A
• MyVariant Identifiers: chr11:g.67353673G>A (hg19) ; chr11:g.67586202G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586202G>A , CM000673.2:g.67586202G>A	GRCh38
NC_000011.9:g.67353673G>A , CM000673.1:g.67353673G>A	GRCh37
NC_000011.8:g.67110249G>A	NCBI36
NG_012075.1:g.7608G>A , LRG_723:g.7608G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.337-187G>A	ENSP00000381604.1:n.337-187G>A
ENST00000398606.10:c.435G>A MANE Select	ENSP00000381607.3:p.Val145=
ENST00000646888.1:c.*151G>A	ENSP00000494477.1:n.*151G>A
ENST00000398603.5:c.337-187G>A	ENSP00000381604.1:n.337-187G>A
ENST00000398606.7:c.435G>A	ENSP00000381607.3:p.Val145=
ENST00000467591.1:n.546G>A
ENST00000494593.1:n.1230G>A
ENST00000495996.1:c.99G>A	ENSP00000484686.1:p.Val33=
ENST00000498765.5:c.498G>A
NM_000852.3:c.435G>A , LRG_723t1:c.435G>A	NP_000843.1:p.Val145=
NM_000852.4:c.435G>A MANE Select	NP_000843.1:p.Val145=