Canonical Allele Identifier: CA224155328

Gene: GSTP1

Linked Data

• dbSNP Id: rs777261816
• gnomAD v3: 11-67586397-C-G
• gnomAD v4: 11-67586397-C-G
• MyVariant Identifiers: chr11:g.67353868C>G (hg19) ; chr11:g.67586397C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586397C>G , CM000673.2:g.67586397C>G	GRCh38
NC_000011.9:g.67353868C>G , CM000673.1:g.67353868C>G	GRCh37
NC_000011.8:g.67110444C>G	NCBI36
NG_012075.1:g.7803C>G , LRG_723:g.7803C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.345C>G	ENSP00000381604.1:p.Phe115Leu
ENST00000398606.10:c.453C>G MANE Select	ENSP00000381607.3:p.Phe151Leu
ENST00000646888.1:c.*169C>G	ENSP00000494477.1:n.*169C>G
ENST00000398603.5:c.345C>G	ENSP00000381604.1:p.Phe115Leu
ENST00000398606.7:c.453C>G	ENSP00000381607.3:p.Phe151Leu
ENST00000467591.1:n.564C>G
ENST00000494593.1:n.1425C>G
ENST00000495996.1:c.179C>G	ENSP00000484686.1:p.Ser60Trp
ENST00000498765.5:c.516C>G
NM_000852.3:c.453C>G , LRG_723t1:c.453C>G	NP_000843.1:p.Phe151Leu
NM_000852.4:c.453C>G MANE Select	NP_000843.1:p.Phe151Leu