Canonical Allele Identifier: CA381518012

Gene: GSTP1

Linked Data

• dbSNP Id: rs1401936187
• gnomAD v2: 11-67352243-G-C
• gnomAD v4: 11-67584772-G-C
• MyVariant Identifiers: chr11:g.67352243G>C (hg19) ; chr11:g.67584772G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67584772G>C , CM000673.2:g.67584772G>C	GRCh38
NC_000011.9:g.67352243G>C , CM000673.1:g.67352243G>C	GRCh37
NC_000011.8:g.67108819G>C	NCBI36
NG_012075.1:g.6178G>C , LRG_723:g.6178G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.232G>C	ENSP00000381604.1:p.Gly78Arg
ENST00000398606.10:c.232G>C MANE Select	ENSP00000381607.3:p.Gly78Arg
ENST00000646888.1:c.125G>C	ENSP00000494477.1:p.Trp42Ser
ENST00000398603.5:c.232G>C	ENSP00000381604.1:p.Gly78Arg
ENST00000398606.7:c.232G>C	ENSP00000381607.3:p.Gly78Arg
ENST00000489040.1:n.231G>C
ENST00000494593.1:n.662G>C
ENST00000498765.5:c.195G>C
NM_000852.3:c.232G>C , LRG_723t1:c.232G>C	NP_000843.1:p.Gly78Arg
NM_000852.4:c.232G>C MANE Select	NP_000843.1:p.Gly78Arg