Canonical Allele Identifier: CA381521069

Gene: GSTP1

Linked Data

• MyVariant Identifiers: chr11:g.67353636T>A (hg19) ; chr11:g.67586165T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586165T>A , CM000673.2:g.67586165T>A	GRCh38
NC_000011.9:g.67353636T>A , CM000673.1:g.67353636T>A	GRCh37
NC_000011.8:g.67110212T>A	NCBI36
NG_012075.1:g.7571T>A , LRG_723:g.7571T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.337-224T>A	ENSP00000381604.1:n.337-224T>A
ENST00000398606.10:c.398T>A MANE Select	ENSP00000381607.3:p.Leu133Gln
ENST00000646888.1:c.*114T>A	ENSP00000494477.1:n.*114T>A
ENST00000398603.5:c.337-224T>A	ENSP00000381604.1:n.337-224T>A
ENST00000398606.7:c.398T>A	ENSP00000381607.3:p.Leu133Gln
ENST00000467591.1:n.509T>A
ENST00000494593.1:n.1193T>A
ENST00000495996.1:c.62T>A	ENSP00000484686.1:p.Leu21Gln
ENST00000498765.5:c.461T>A
NM_000852.3:c.398T>A , LRG_723t1:c.398T>A	NP_000843.1:p.Leu133Gln
NM_000852.4:c.398T>A MANE Select	NP_000843.1:p.Leu133Gln