Canonical Allele Identifier: CA6142876

Gene: GSTP1

Linked Data

• dbSNP Id: rs71534294
• ExAC: 11:67353887 G / C
• gnomAD v2: 11-67353887-G-C
• gnomAD v3: 11-67586416-G-C
• gnomAD v4: 11-67586416-G-C
• MyVariant Identifiers: chr11:g.67353887G>C (hg19) ; chr11:g.67586416G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67586416G>C , CM000673.2:g.67586416G>C	GRCh38
NC_000011.9:g.67353887G>C , CM000673.1:g.67353887G>C	GRCh37
NC_000011.8:g.67110463G>C	NCBI36
NG_012075.1:g.7822G>C , LRG_723:g.7822G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398603.6:c.364G>C	ENSP00000381604.1:p.Asp122His
ENST00000398606.10:c.472G>C MANE Select	ENSP00000381607.3:p.Asp158His
ENST00000646888.1:c.*188G>C	ENSP00000494477.1:n.*188G>C
ENST00000398603.5:c.364G>C	ENSP00000381604.1:p.Asp122His
ENST00000398606.7:c.472G>C	ENSP00000381607.3:p.Asp158His
ENST00000467591.1:n.583G>C
ENST00000494593.1:n.1444G>C
ENST00000495996.1:c.198G>C	ENSP00000484686.1:p.Trp66Cys
ENST00000498765.5:c.535G>C
NM_000852.3:c.472G>C , LRG_723t1:c.472G>C	NP_000843.1:p.Asp158His
NM_000852.4:c.472G>C MANE Select	NP_000843.1:p.Asp158His