Canonical Allele Identifier: CA6142724

Gene: GSTP1

Linked Data

• dbSNP Id: rs570140337
• ExAC: 11:67352092 T / G
• gnomAD v2: 11-67352092-T-G
• gnomAD v3: 11-67584621-T-G
• gnomAD v4: 11-67584621-T-G
• MyVariant Identifiers: chr11:g.67352092T>G (hg19) ; chr11:g.67584621T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67584621T>G , CM000673.2:g.67584621T>G	GRCh38
NC_000011.9:g.67352092T>G , CM000673.1:g.67352092T>G	GRCh37
NC_000011.8:g.67108668T>G	NCBI36
NG_012075.1:g.6027T>G , LRG_723:g.6027T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.144+51T>G	ENSP00000381604.1:n.144+51T>G
ENST00000398606.10:c.144+51T>G MANE Select	ENSP00000381607.3:n.144+51T>G
ENST00000646888.1:c.38-64T>G	ENSP00000494477.1:n.38-64T>G
ENST00000398603.5:c.144+51T>G	ENSP00000381604.1:n.144+51T>G
ENST00000398606.7:c.144+51T>G	ENSP00000381607.3:n.144+51T>G
ENST00000489040.1:n.143+51T>G
ENST00000494593.1:n.511T>G
ENST00000498765.5:c.107+51T>G
NM_000852.3:c.144+51T>G , LRG_723t1:c.144+51T>G	NP_000843.1:n.144+51T>G
NM_000852.4:c.144+51T>G MANE Select	NP_000843.1:n.144+51T>G