Canonical Allele Identifier: CA1980215142

Gene: GSTP1

Linked Data

• dbSNP Id: rs1867452921

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67585509_67585510insA , CM000673.2:g.67585509_67585510insA	GRCh38
NC_000011.9:g.67352980_67352981insA , CM000673.1:g.67352980_67352981insA	GRCh37
NC_000011.8:g.67109556_67109557insA	NCBI36
NG_012075.1:g.6915_6916insA , LRG_723:g.6915_6916insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.336+268_336+269insA	ENSP00000381604.1:n.336+268_336+269insA
ENST00000398606.10:c.336+268_336+269insA MANE Select	ENSP00000381607.3:n.336+268_336+269insA
ENST00000646888.1:c.*52+268_*52+269insA	ENSP00000494477.1:n.*52+268_*52+269insA
ENST00000398603.5:c.336+268_336+269insA	ENSP00000381604.1:n.336+268_336+269insA
ENST00000398606.7:c.336+268_336+269insA	ENSP00000381607.3:n.336+268_336+269insA
ENST00000467591.1:n.447+268_447+269insA
ENST00000494593.1:n.1131+268_1131+269insA
ENST00000498765.5:c.399+268_399+269insA
NM_000852.3:c.336+268_336+269insA , LRG_723t1:c.336+268_336+269insA	NP_000843.1:n.336+268_336+269insA
NM_000852.4:c.336+268_336+269insA MANE Select	NP_000843.1:n.336+268_336+269insA