Canonical Allele Identifier: CA2724396375
Gene: GSTP1 HGNC NCBI

Linked Data

dbSNP Id: rs2134394481

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67585248_67585249insCTGCCCGGGCAACTGAAGCC , CM000673.2:g.67585248_67585249insCTGCCCGGGCAACTGAAGCC GRCh38
NC_000011.9:g.67352719_67352720insCTGCCCGGGCAACTGAAGCC , CM000673.1:g.67352719_67352720insCTGCCCGGGCAACTGAAGCC GRCh37
NC_000011.8:g.67109295_67109296insCTGCCCGGGCAACTGAAGCC NCBI36
NG_012075.1:g.6654_6655insCTGCCCGGGCAACTGAAGCC , LRG_723:g.6654_6655insCTGCCCGGGCAACTGAAGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.336+7_336+8insCTGCCCGGGCAACTGAAGCC ENSP00000381604.1:n.336+7_336+8insCTGCCCGGGCAACTGAAGCC
ENST00000398606.10:c.336+7_336+8insCTGCCCGGGCAACTGAAGCC MANE Select ENSP00000381607.3:n.336+7_336+8insCTGCCCGGGCAACTGAAGCC
ENST00000646888.1:c.*52+7_*52+8insCTGCCCGGGCAACTGAAGCC ENSP00000494477.1:n.*52+7_*52+8insCTGCCCGGGCAACTGAAGCC
ENST00000398603.5:c.336+7_336+8insCTGCCCGGGCAACTGAAGCC ENSP00000381604.1:n.336+7_336+8insCTGCCCGGGCAACTGAAGCC
ENST00000398606.7:c.336+7_336+8insCTGCCCGGGCAACTGAAGCC ENSP00000381607.3:n.336+7_336+8insCTGCCCGGGCAACTGAAGCC
ENST00000467591.1:n.447+7_447+8insCTGCCCGGGCAACTGAAGCC
ENST00000494593.1:n.1131+7_1131+8insCTGCCCGGGCAACTGAAGCC
ENST00000498765.5:c.399+7_399+8insCTGCCCGGGCAACTGAAGCC
NM_000852.3:c.336+7_336+8insCTGCCCGGGCAACTGAAGCC , LRG_723t1:c.336+7_336+8insCTGCCCGGGCAACTGAAGCC NP_000843.1:n.336+7_336+8insCTGCCCGGGCAACTGAAGCC
NM_000852.4:c.336+7_336+8insCTGCCCGGGCAACTGAAGCC MANE Select NP_000843.1:n.336+7_336+8insCTGCCCGGGCAACTGAAGCC