Canonical Allele Identifier: CA1980215069

Gene: GSTP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67585446_67585448delinsAAG , CM000673.2:g.67585446_67585448delinsAAG	GRCh38
NC_000011.9:g.67352917_67352919delinsAAG , CM000673.1:g.67352917_67352919delinsAAG	GRCh37
NC_000011.8:g.67109493_67109495delinsAAG	NCBI36
NG_012075.1:g.6852_6854delinsAAG , LRG_723:g.6852_6854delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.336+205_336+207delinsAAG	ENSP00000381604.1:n.336+205_336+207delinsAAG
ENST00000398606.10:c.336+205_336+207delinsAAG MANE Select	ENSP00000381607.3:n.336+205_336+207delinsAAG
ENST00000646888.1:c.*52+205_*52+207delinsAAG	ENSP00000494477.1:n.*52+205_*52+207delinsAAG
ENST00000398603.5:c.336+205_336+207delinsAAG	ENSP00000381604.1:n.336+205_336+207delinsAAG
ENST00000398606.7:c.336+205_336+207delinsAAG	ENSP00000381607.3:n.336+205_336+207delinsAAG
ENST00000467591.1:n.447+205_447+207delinsAAG
ENST00000494593.1:n.1131+205_1131+207delinsAAG
ENST00000498765.5:c.399+205_399+207delinsAAG
NM_000852.3:c.336+205_336+207delinsAAG , LRG_723t1:c.336+205_336+207delinsAAG	NP_000843.1:n.336+205_336+207delinsAAG
NM_000852.4:c.336+205_336+207delinsAAG MANE Select	NP_000843.1:n.336+205_336+207delinsAAG