Canonical Allele Identifier: CA381522817

Gene: GSTP1

Linked Data

• MyVariant Identifiers: chr11:g.67353935T>G (hg19) ; chr11:g.67586464T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586464T>G , CM000673.2:g.67586464T>G	GRCh38
NC_000011.9:g.67353935T>G , CM000673.1:g.67353935T>G	GRCh37
NC_000011.8:g.67110511T>G	NCBI36
NG_012075.1:g.7870T>G , LRG_723:g.7870T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.412T>G	ENSP00000381604.1:p.Phe138Val
ENST00000398606.10:c.520T>G MANE Select	ENSP00000381607.3:p.Phe174Val
ENST00000646888.1:c.*236T>G	ENSP00000494477.1:n.*236T>G
ENST00000398603.5:c.412T>G	ENSP00000381604.1:p.Phe138Val
ENST00000398606.7:c.520T>G	ENSP00000381607.3:p.Phe174Val
ENST00000467591.1:n.631T>G
ENST00000494593.1:n.1492T>G
ENST00000498765.5:c.583T>G
NM_000852.3:c.520T>G , LRG_723t1:c.520T>G	NP_000843.1:p.Phe174Val
NM_000852.4:c.520T>G MANE Select	NP_000843.1:p.Phe174Val