Canonical Allele Identifier: CA475396032

Gene: GSTP1

Linked Data

• dbSNP Id: rs1381977953
• gnomAD v2: 11-67353625-T-G
• gnomAD v3: 11-67586154-T-G
• gnomAD v4: 11-67586154-T-G
• MyVariant Identifiers: chr11:g.67353625T>G (hg19) ; chr11:g.67586154T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586154T>G , CM000673.2:g.67586154T>G	GRCh38
NC_000011.9:g.67353625T>G , CM000673.1:g.67353625T>G	GRCh37
NC_000011.8:g.67110201T>G	NCBI36
NG_012075.1:g.7560T>G , LRG_723:g.7560T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.337-235T>G	ENSP00000381604.1:n.337-235T>G
ENST00000398606.10:c.387T>G MANE Select	ENSP00000381607.3:p.Pro129=
ENST00000646888.1:c.*103T>G	ENSP00000494477.1:n.*103T>G
ENST00000398603.5:c.337-235T>G	ENSP00000381604.1:n.337-235T>G
ENST00000398606.7:c.387T>G	ENSP00000381607.3:p.Pro129=
ENST00000467591.1:n.498T>G
ENST00000494593.1:n.1182T>G
ENST00000495996.1:c.51T>G	ENSP00000484686.1:p.Pro17=
ENST00000498765.5:c.450T>G
NM_000852.3:c.387T>G , LRG_723t1:c.387T>G	NP_000843.1:p.Pro129=
NM_000852.4:c.387T>G MANE Select	NP_000843.1:p.Pro129=