Canonical Allele Identifier: CA6142822
Gene: GSTP1 HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.67586111G>A
GRCh37 chr11:g.67353582G>A
Revel Score:
ENST00000398606 (MANE Select) 0.173
gnomAD v2:
11:67353582 G / A
gnomAD v4:
chr11-67586111-G-A
Joint Max Group AF 0.00000443 (AFR)
Exomes Max Group AF 0.0000099 (AFR)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67586111G>A , CM000673.2:g.67586111G>A GRCh38
NC_000011.9:g.67353582G>A , CM000673.1:g.67353582G>A GRCh37
NC_000011.8:g.67110158G>A NCBI36
NG_012075.1:g.7517G>A , LRG_723:g.7517G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398603.6:c.337-278G>A ENSP00000381604.1:n.337-278G>A
ENST00000398606.10:c.344G>A MANE Select ENSP00000381607.3:p.Gly115Asp
ENST00000646888.1:c.*60G>A ENSP00000494477.1:n.*60G>A
ENST00000398603.5:c.337-278G>A ENSP00000381604.1:n.337-278G>A
ENST00000398606.7:c.344G>A ENSP00000381607.3:p.Gly115Asp
ENST00000467591.1:n.455G>A
ENST00000494593.1:n.1139G>A
ENST00000495996.1:c.8G>A ENSP00000484686.1:p.Gly3Asp
ENST00000498765.5:c.407G>A
NM_000852.3:c.344G>A , LRG_723t1:c.344G>A NP_000843.1:p.Gly115Asp
NM_000852.4:c.344G>A MANE Select NP_000843.1:p.Gly115Asp
Search 100 bp 5'
Search 100 bp 3'