Canonical Allele Identifier: CA475395325

Gene: GSTP1

Linked Data

• dbSNP Id: rs1227612614
• gnomAD v2: 11-67353131-T-TGTGTGC
• gnomAD v3: 11-67585660-T-TGTGTGC
• gnomAD v4: 11-67585660-T-TGTGTGC
• MyVariant Identifiers: chr11:g.67353131_67353132insGTGTGC (hg19) ; chr11:g.67585660_67585661insGTGTGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67585662_67585667dup , CM000673.2:g.67585662_67585667dup	GRCh38
NC_000011.9:g.67353133_67353138dup , CM000673.1:g.67353133_67353138dup	GRCh37
NC_000011.8:g.67109709_67109714dup	NCBI36
NG_012075.1:g.7068_7073dup , LRG_723:g.7068_7073dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.336+421_336+426dup	ENSP00000381604.1:n.336+421_336+426dup
ENST00000398606.10:c.336+421_336+426dup MANE Select	ENSP00000381607.3:n.336+421_336+426dup
ENST00000646888.1:c.*52+421_*52+426dup	ENSP00000494477.1:n.*52+421_*52+426dup
ENST00000398603.5:c.336+421_336+426dup	ENSP00000381604.1:n.336+421_336+426dup
ENST00000398606.7:c.336+421_336+426dup	ENSP00000381607.3:n.336+421_336+426dup
ENST00000467591.1:n.447+421_447+426dup
ENST00000494593.1:n.1131+421_1131+426dup
ENST00000498765.5:c.399+421_399+426dup
NM_000852.3:c.336+421_336+426dup , LRG_723t1:c.336+421_336+426dup	NP_000843.1:n.336+421_336+426dup
NM_000852.4:c.336+421_336+426dup MANE Select	NP_000843.1:n.336+421_336+426dup