Canonical Allele Identifier: CA381521002

Gene: GSTP1

Linked Data

• MyVariant Identifiers: chr11:g.67353627T>G (hg19) ; chr11:g.67586156T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586156T>G , CM000673.2:g.67586156T>G	GRCh38
NC_000011.9:g.67353627T>G , CM000673.1:g.67353627T>G	GRCh37
NC_000011.8:g.67110203T>G	NCBI36
NG_012075.1:g.7562T>G , LRG_723:g.7562T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.337-233T>G	ENSP00000381604.1:n.337-233T>G
ENST00000398606.10:c.389T>G MANE Select	ENSP00000381607.3:p.Phe130Cys
ENST00000646888.1:c.*105T>G	ENSP00000494477.1:n.*105T>G
ENST00000398603.5:c.337-233T>G	ENSP00000381604.1:n.337-233T>G
ENST00000398606.7:c.389T>G	ENSP00000381607.3:p.Phe130Cys
ENST00000467591.1:n.500T>G
ENST00000494593.1:n.1184T>G
ENST00000495996.1:c.53T>G	ENSP00000484686.1:p.Phe18Cys
ENST00000498765.5:c.452T>G
NM_000852.3:c.389T>G , LRG_723t1:c.389T>G	NP_000843.1:p.Phe130Cys
NM_000852.4:c.389T>G MANE Select	NP_000843.1:p.Phe130Cys