Canonical Allele Identifier: CA599909718

Gene: GSTP1

Linked Data

• dbSNP Id: rs1377779849
• gnomAD v2: 11-67353094-C-G
• gnomAD v3: 11-67585623-C-G
• gnomAD v4: 11-67585623-C-G
• MyVariant Identifiers: chr11:g.67353094C>G (hg19) ; chr11:g.67585623C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67585623C>G , CM000673.2:g.67585623C>G	GRCh38
NC_000011.9:g.67353094C>G , CM000673.1:g.67353094C>G	GRCh37
NC_000011.8:g.67109670C>G	NCBI36
NG_012075.1:g.7029C>G , LRG_723:g.7029C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000398603.6:c.336+382C>G	ENSP00000381604.1:n.336+382C>G
ENST00000398606.10:c.336+382C>G MANE Select	ENSP00000381607.3:n.336+382C>G
ENST00000646888.1:c.*52+382C>G	ENSP00000494477.1:n.*52+382C>G
ENST00000398603.5:c.336+382C>G	ENSP00000381604.1:n.336+382C>G
ENST00000398606.7:c.336+382C>G	ENSP00000381607.3:n.336+382C>G
ENST00000467591.1:n.447+382C>G
ENST00000494593.1:n.1131+382C>G
ENST00000498765.5:c.399+382C>G
NM_000852.3:c.336+382C>G , LRG_723t1:c.336+382C>G	NP_000843.1:n.336+382C>G
NM_000852.4:c.336+382C>G MANE Select	NP_000843.1:n.336+382C>G