Canonical Allele Identifier: CA1980215091

Gene: GSTP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67585459_67585460delinsTG , CM000673.2:g.67585459_67585460delinsTG	GRCh38
NC_000011.9:g.67352930_67352931delinsTG , CM000673.1:g.67352930_67352931delinsTG	GRCh37
NC_000011.8:g.67109506_67109507delinsTG	NCBI36
NG_012075.1:g.6865_6866delinsTG , LRG_723:g.6865_6866delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.336+218_336+219delinsTG	ENSP00000381604.1:n.336+218_336+219delinsTG
ENST00000398606.10:c.336+218_336+219delinsTG MANE Select	ENSP00000381607.3:n.336+218_336+219delinsTG
ENST00000646888.1:c.*52+218_*52+219delinsTG	ENSP00000494477.1:n.*52+218_*52+219delinsTG
ENST00000398603.5:c.336+218_336+219delinsTG	ENSP00000381604.1:n.336+218_336+219delinsTG
ENST00000398606.7:c.336+218_336+219delinsTG	ENSP00000381607.3:n.336+218_336+219delinsTG
ENST00000467591.1:n.447+218_447+219delinsTG
ENST00000494593.1:n.1131+218_1131+219delinsTG
ENST00000498765.5:c.399+218_399+219delinsTG
NM_000852.3:c.336+218_336+219delinsTG , LRG_723t1:c.336+218_336+219delinsTG	NP_000843.1:n.336+218_336+219delinsTG
NM_000852.4:c.336+218_336+219delinsTG MANE Select	NP_000843.1:n.336+218_336+219delinsTG