Canonical Allele Identifier: CA390507639
Gene: GSTZ1 HGNC NCBI

Linked Data

dbSNP Id: rs1594824886

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77327528T>G , CM000676.2:g.77327528T>G GRCh38
NC_000014.8:g.77793871T>G , CM000676.1:g.77793871T>G GRCh37
NC_000014.7:g.76863624T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000216465.10:c.192T>G MANE Select ENSP00000216465.5:p.Ile64Met
ENST00000216465.9:c.192T>G ENSP00000216465.5:p.Ile64Met
ENST00000349555.7:c.192T>G ENSP00000314404.5:p.Ile64Met
ENST00000361389.8:c.27T>G ENSP00000354959.4:p.Ile9Met
ENST00000393734.5:c.27T>G ENSP00000377335.1:p.Ile9Met
ENST00000553431.5:n.323T>G
ENST00000553586.5:c.195T>G ENSP00000451976.1:p.Ile65Met
ENST00000553838.5:n.362T>G
ENST00000554279.5:c.174+18T>G ENSP00000452498.1:n.174+18T>G
ENST00000554846.5:c.27T>G ENSP00000452531.1:p.Ile9Met
ENST00000555093.1:n.4241T>G
ENST00000555583.1:c.27T>G ENSP00000452346.1:p.Ile9Met
ENST00000556627.5:c.136-384T>G ENSP00000450487.1:n.136-384T>G
ENST00000556914.5:n.272T>G
ENST00000557053.5:c.27T>G ENSP00000451150.1:p.Ile9Met
ENST00000557639.5:c.27T>G ENSP00000451927.1:p.Ile9Met
NM_001312660.1:c.27T>G NP_001299589.1:p.Ile9Met
NM_001513.3:c.27T>G NP_001504.2:p.Ile9Met
NM_145870.2:c.192T>G NP_665877.1:p.Ile64Met
NM_145871.2:c.192T>G NP_665878.2:p.Ile64Met
XM_005267559.2:c.27T>G XP_005267616.1:p.Ile9Met
XM_011536670.1:c.-285T>G XP_011534972.1:n.-285T>G
XM_011536671.1:c.195T>G XP_011534973.1:p.Ile65Met
NM_001363703.1:c.195T>G NP_001350632.1:p.Ile65Met
XM_011536670.2:c.-285T>G XP_011534972.1:n.-285T>G
XM_011536671.2:c.195T>G XP_011534973.1:p.Ile65Met
XM_024449549.1:c.-285T>G XP_024305317.1:n.-285T>G
XM_024449550.1:c.27T>G XP_024305318.1:p.Ile9Met
XM_024449551.1:c.27T>G XP_024305319.1:p.Ile9Met
XM_024449552.1:c.27T>G XP_024305320.1:p.Ile9Met
NM_145870.3:c.192T>G MANE Select NP_665877.1:p.Ile64Met
NM_001312660.2:c.27T>G NP_001299589.1:p.Ile9Met
NM_001363703.2:c.195T>G NP_001350632.1:p.Ile65Met
NM_145871.3:c.192T>G NP_665878.2:p.Ile64Met