Canonical Allele Identifier: CA6142834

Gene: GSTP1

Linked Data

• dbSNP Id: rs778023522
• ExAC: 11:67353633 C / T
• gnomAD v2: 11-67353633-C-T
• gnomAD v3: 11-67586162-C-T
• gnomAD v4: 11-67586162-C-T
• MyVariant Identifiers: chr11:g.67353633C>T (hg19) ; chr11:g.67586162C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586162C>T , CM000673.2:g.67586162C>T	GRCh38
NC_000011.9:g.67353633C>T , CM000673.1:g.67353633C>T	GRCh37
NC_000011.8:g.67110209C>T	NCBI36
NG_012075.1:g.7568C>T , LRG_723:g.7568C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.337-227C>T	ENSP00000381604.1:n.337-227C>T
ENST00000398606.10:c.395C>T MANE Select	ENSP00000381607.3:p.Thr132Ile
ENST00000646888.1:c.*111C>T	ENSP00000494477.1:n.*111C>T
ENST00000398603.5:c.337-227C>T	ENSP00000381604.1:n.337-227C>T
ENST00000398606.7:c.395C>T	ENSP00000381607.3:p.Thr132Ile
ENST00000467591.1:n.506C>T
ENST00000494593.1:n.1190C>T
ENST00000495996.1:c.59C>T	ENSP00000484686.1:p.Thr20Ile
ENST00000498765.5:c.458C>T
NM_000852.3:c.395C>T , LRG_723t1:c.395C>T	NP_000843.1:p.Thr132Ile
NM_000852.4:c.395C>T MANE Select	NP_000843.1:p.Thr132Ile