Canonical Allele Identifier: CA658821155

Gene: GSTP1

Linked Data

• ClinVar Variation Id: 496691
• ClinVar RCV Id: RCV000677248
• dbSNP Id: rs1555022268

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67585320_67585321delinsCA , CM000673.2:g.67585320_67585321delinsCA	GRCh38
NC_000011.9:g.67352791_67352792delinsCA , CM000673.1:g.67352791_67352792delinsCA	GRCh37
NC_000011.8:g.67109367_67109368delinsCA	NCBI36
NG_012075.1:g.6726_6727delinsCA , LRG_723:g.6726_6727delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.336+79_336+80delinsCA	ENSP00000381604.1:n.336+79_336+80delinsCA
ENST00000398606.10:c.336+79_336+80delinsCA MANE Select	ENSP00000381607.3:n.336+79_336+80delinsCA
ENST00000646888.1:c.*52+79_*52+80delinsCA	ENSP00000494477.1:n.*52+79_*52+80delinsCA
ENST00000398603.5:c.336+79_336+80delinsCA	ENSP00000381604.1:n.336+79_336+80delinsCA
ENST00000398606.7:c.336+79_336+80delinsCA	ENSP00000381607.3:n.336+79_336+80delinsCA
ENST00000467591.1:n.447+79_447+80delinsCA
ENST00000494593.1:n.1131+79_1131+80delinsCA
ENST00000498765.5:c.399+79_399+80delinsCA
NM_000852.3:c.336+79_336+80delinsCA , LRG_723t1:c.336+79_336+80delinsCA	NP_000843.1:n.336+79_336+80delinsCA
NM_000852.4:c.336+79_336+80delinsCA MANE Select	NP_000843.1:n.336+79_336+80delinsCA