Canonical Allele Identifier: CA381522276

Gene: GSTP1

Linked Data

• MyVariant Identifiers: chr11:g.67353866T>G (hg19) ; chr11:g.67586395T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586395T>G , CM000673.2:g.67586395T>G	GRCh38
NC_000011.9:g.67353866T>G , CM000673.1:g.67353866T>G	GRCh37
NC_000011.8:g.67110442T>G	NCBI36
NG_012075.1:g.7801T>G , LRG_723:g.7801T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.343T>G	ENSP00000381604.1:p.Phe115Val
ENST00000398606.10:c.451T>G MANE Select	ENSP00000381607.3:p.Phe151Val
ENST00000646888.1:c.*167T>G	ENSP00000494477.1:n.*167T>G
ENST00000398603.5:c.343T>G	ENSP00000381604.1:p.Phe115Val
ENST00000398606.7:c.451T>G	ENSP00000381607.3:p.Phe151Val
ENST00000467591.1:n.562T>G
ENST00000494593.1:n.1423T>G
ENST00000495996.1:c.177T>G	ENSP00000484686.1:p.Pro59=
ENST00000498765.5:c.514T>G
NM_000852.3:c.451T>G , LRG_723t1:c.451T>G	NP_000843.1:p.Phe151Val
NM_000852.4:c.451T>G MANE Select	NP_000843.1:p.Phe151Val