Canonical Allele Identifier: CA1980215020

Gene: GSTP1

Linked Data

• dbSNP Id: rs1867451371
• gnomAD v4: 11-67585386-GCCCAGGGGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67585388_67585396del , CM000673.2:g.67585388_67585396del	GRCh38
NC_000011.9:g.67352859_67352867del , CM000673.1:g.67352859_67352867del	GRCh37
NC_000011.8:g.67109435_67109443del	NCBI36
NG_012075.1:g.6794_6802del , LRG_723:g.6794_6802del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.336+147_336+155del	ENSP00000381604.1:n.336+147_336+155del
ENST00000398606.10:c.336+147_336+155del MANE Select	ENSP00000381607.3:n.336+147_336+155del
ENST00000646888.1:c.*52+147_*52+155del	ENSP00000494477.1:n.*52+147_*52+155del
ENST00000398603.5:c.336+147_336+155del	ENSP00000381604.1:n.336+147_336+155del
ENST00000398606.7:c.336+147_336+155del	ENSP00000381607.3:n.336+147_336+155del
ENST00000467591.1:n.447+147_447+155del
ENST00000494593.1:n.1131+147_1131+155del
ENST00000498765.5:c.399+147_399+155del
NM_000852.3:c.336+147_336+155del , LRG_723t1:c.336+147_336+155del	NP_000843.1:n.336+147_336+155del
NM_000852.4:c.336+147_336+155del MANE Select	NP_000843.1:n.336+147_336+155del