Canonical Allele Identifier: CA390507582
Gene: GSTZ1 HGNC NCBI

Linked Data

dbSNP Id: rs1438780672

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77327517A>G , CM000676.2:g.77327517A>G GRCh38
NC_000014.8:g.77793860A>G , CM000676.1:g.77793860A>G GRCh37
NC_000014.7:g.76863613A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000216465.10:c.181A>G MANE Select ENSP00000216465.5:p.Thr61Ala
ENST00000216465.9:c.181A>G ENSP00000216465.5:p.Thr61Ala
ENST00000349555.7:c.181A>G ENSP00000314404.5:p.Thr61Ala
ENST00000361389.8:c.16A>G ENSP00000354959.4:p.Thr6Ala
ENST00000393734.5:c.16A>G ENSP00000377335.1:p.Thr6Ala
ENST00000553431.5:n.312A>G
ENST00000553586.5:c.184A>G ENSP00000451976.1:p.Thr62Ala
ENST00000553838.5:n.351A>G
ENST00000554279.5:c.174+7A>G ENSP00000452498.1:n.174+7A>G
ENST00000554846.5:c.16A>G ENSP00000452531.1:p.Thr6Ala
ENST00000555093.1:n.4230A>G
ENST00000555583.1:c.16A>G ENSP00000452346.1:p.Thr6Ala
ENST00000556627.5:c.136-395A>G ENSP00000450487.1:n.136-395A>G
ENST00000556914.5:n.261A>G
ENST00000557053.5:c.16A>G ENSP00000451150.1:p.Thr6Ala
ENST00000557639.5:c.16A>G ENSP00000451927.1:p.Thr6Ala
NM_001312660.1:c.16A>G NP_001299589.1:p.Thr6Ala
NM_001513.3:c.16A>G NP_001504.2:p.Thr6Ala
NM_145870.2:c.181A>G NP_665877.1:p.Thr61Ala
NM_145871.2:c.181A>G NP_665878.2:p.Thr61Ala
XM_005267559.2:c.16A>G XP_005267616.1:p.Thr6Ala
XM_011536670.1:c.-296A>G XP_011534972.1:n.-296A>G
XM_011536671.1:c.184A>G XP_011534973.1:p.Thr62Ala
NM_001363703.1:c.184A>G NP_001350632.1:p.Thr62Ala
XM_011536670.2:c.-296A>G XP_011534972.1:n.-296A>G
XM_011536671.2:c.184A>G XP_011534973.1:p.Thr62Ala
XM_024449549.1:c.-296A>G XP_024305317.1:n.-296A>G
XM_024449550.1:c.16A>G XP_024305318.1:p.Thr6Ala
XM_024449551.1:c.16A>G XP_024305319.1:p.Thr6Ala
XM_024449552.1:c.16A>G XP_024305320.1:p.Thr6Ala
NM_145870.3:c.181A>G MANE Select NP_665877.1:p.Thr61Ala
NM_001312660.2:c.16A>G NP_001299589.1:p.Thr6Ala
NM_001363703.2:c.184A>G NP_001350632.1:p.Thr62Ala
NM_145871.3:c.181A>G NP_665878.2:p.Thr61Ala