Canonical Allele Identifier: CA600237055

Gene: GSTP1

Linked Data

• dbSNP Id: rs764284088
• gnomAD v2: 11-67353848-C-A
• gnomAD v4: 11-67586377-C-A
• MyVariant Identifiers: chr11:g.67353848C>A (hg19) ; chr11:g.67586377C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586377C>A , CM000673.2:g.67586377C>A	GRCh38
NC_000011.9:g.67353848C>A , CM000673.1:g.67353848C>A	GRCh37
NC_000011.8:g.67110424C>A	NCBI36
NG_012075.1:g.7783C>A , LRG_723:g.7783C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.337-12C>A	ENSP00000381604.1:n.337-12C>A
ENST00000398606.10:c.445-12C>A MANE Select	ENSP00000381607.3:n.445-12C>A
ENST00000646888.1:c.*161-12C>A	ENSP00000494477.1:n.*161-12C>A
ENST00000398603.5:c.337-12C>A	ENSP00000381604.1:n.337-12C>A
ENST00000398606.7:c.445-12C>A	ENSP00000381607.3:n.445-12C>A
ENST00000467591.1:n.556-12C>A
ENST00000494593.1:n.1405C>A
ENST00000495996.1:c.171-12C>A	ENSP00000484686.1:n.171-12C>A
ENST00000498765.5:c.508-12C>A
NM_000852.3:c.445-12C>A , LRG_723t1:c.445-12C>A	NP_000843.1:n.445-12C>A
NM_000852.4:c.445-12C>A MANE Select	NP_000843.1:n.445-12C>A