Canonical Allele Identifier: CA390507663
Gene: GSTZ1 HGNC NCBI

Linked Data

dbSNP Id: rs2139575412

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77327533G>A , CM000676.2:g.77327533G>A GRCh38
NC_000014.8:g.77793876G>A , CM000676.1:g.77793876G>A GRCh37
NC_000014.7:g.76863629G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000216465.10:c.197G>A MANE Select ENSP00000216465.5:p.Gly66Glu
ENST00000216465.9:c.197G>A ENSP00000216465.5:p.Gly66Glu
ENST00000349555.7:c.197G>A ENSP00000314404.5:p.Gly66Glu
ENST00000361389.8:c.32G>A ENSP00000354959.4:p.Gly11Glu
ENST00000393734.5:c.32G>A ENSP00000377335.1:p.Gly11Glu
ENST00000553431.5:n.328G>A
ENST00000553586.5:c.200G>A ENSP00000451976.1:p.Gly67Glu
ENST00000553838.5:n.367G>A
ENST00000554279.5:c.174+23G>A ENSP00000452498.1:n.174+23G>A
ENST00000554846.5:c.32G>A ENSP00000452531.1:p.Gly11Glu
ENST00000555093.1:n.4246G>A
ENST00000555583.1:c.32G>A ENSP00000452346.1:p.Gly11Glu
ENST00000556627.5:c.136-379G>A ENSP00000450487.1:n.136-379G>A
ENST00000556914.5:n.277G>A
ENST00000557053.5:c.32G>A ENSP00000451150.1:p.Gly11Glu
ENST00000557639.5:c.32G>A ENSP00000451927.1:p.Gly11Glu
NM_001312660.1:c.32G>A NP_001299589.1:p.Gly11Glu
NM_001513.3:c.32G>A NP_001504.2:p.Gly11Glu
NM_145870.2:c.197G>A NP_665877.1:p.Gly66Glu
NM_145871.2:c.197G>A NP_665878.2:p.Gly66Glu
XM_005267559.2:c.32G>A XP_005267616.1:p.Gly11Glu
XM_011536670.1:c.-280G>A XP_011534972.1:n.-280G>A
XM_011536671.1:c.200G>A XP_011534973.1:p.Gly67Glu
NM_001363703.1:c.200G>A NP_001350632.1:p.Gly67Glu
XM_011536670.2:c.-280G>A XP_011534972.1:n.-280G>A
XM_011536671.2:c.200G>A XP_011534973.1:p.Gly67Glu
XM_024449549.1:c.-280G>A XP_024305317.1:n.-280G>A
XM_024449550.1:c.32G>A XP_024305318.1:p.Gly11Glu
XM_024449551.1:c.32G>A XP_024305319.1:p.Gly11Glu
XM_024449552.1:c.32G>A XP_024305320.1:p.Gly11Glu
NM_145870.3:c.197G>A MANE Select NP_665877.1:p.Gly66Glu
NM_001312660.2:c.32G>A NP_001299589.1:p.Gly11Glu
NM_001363703.2:c.200G>A NP_001350632.1:p.Gly67Glu
NM_145871.3:c.197G>A NP_665878.2:p.Gly66Glu