Canonical Allele Identifier: CA381523018

Gene: GSTP1

Linked Data

• MyVariant Identifiers: chr11:g.67353972C>T (hg19) ; chr11:g.67586501C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586501C>T , CM000673.2:g.67586501C>T	GRCh38
NC_000011.9:g.67353972C>T , CM000673.1:g.67353972C>T	GRCh37
NC_000011.8:g.67110548C>T	NCBI36
NG_012075.1:g.7907C>T , LRG_723:g.7907C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.449C>T	ENSP00000381604.1:p.Ala150Val
ENST00000398606.10:c.557C>T MANE Select	ENSP00000381607.3:p.Ala186Val
ENST00000646888.1:c.*273C>T	ENSP00000494477.1:n.*273C>T
ENST00000398603.5:c.449C>T	ENSP00000381604.1:p.Ala150Val
ENST00000398606.7:c.557C>T	ENSP00000381607.3:p.Ala186Val
ENST00000467591.1:n.668C>T
ENST00000494593.1:n.1529C>T
ENST00000498765.5:c.620C>T
NM_000852.3:c.557C>T , LRG_723t1:c.557C>T	NP_000843.1:p.Ala186Val
NM_000852.4:c.557C>T MANE Select	NP_000843.1:p.Ala186Val