Canonical Allele Identifier: CA2148347125
Gene: GSTZ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77327485_77327486delinsTC , CM000676.2:g.77327485_77327486delinsTC GRCh38
NC_000014.8:g.77793828_77793829delinsTC , CM000676.1:g.77793828_77793829delinsTC GRCh37
NC_000014.7:g.76863581_76863582delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000216465.10:c.149_150delinsTC MANE Select ENSP00000216465.5:p.Phe50=
ENST00000216465.9:c.149_150delinsTC ENSP00000216465.5:p.Phe50=
ENST00000349555.7:c.149_150delinsTC ENSP00000314404.5:p.Phe50=
ENST00000361389.8:c.-17_-16delinsTC ENSP00000354959.4:n.-17_-16delinsTC
ENST00000393734.5:c.-17_-16delinsTC ENSP00000377335.1:n.-17_-16delinsTC
ENST00000553431.5:n.280_281delinsTC
ENST00000553586.5:c.152_153delinsTC ENSP00000451976.1:p.Phe51=
ENST00000553838.5:n.319_320delinsTC
ENST00000554279.5:c.149_150delinsTC ENSP00000452498.1:p.Phe50=
ENST00000554846.5:c.-17_-16delinsTC ENSP00000452531.1:n.-17_-16delinsTC
ENST00000555093.1:n.4198_4199delinsTC
ENST00000555583.1:c.-17_-16delinsTC ENSP00000452346.1:n.-17_-16delinsTC
ENST00000556627.5:c.136-427_136-426delinsTC ENSP00000450487.1:n.136-427_136-426delinsTC
ENST00000556914.5:n.229_230delinsTC
ENST00000557053.5:c.-17_-16delinsTC ENSP00000451150.1:n.-17_-16delinsTC
ENST00000557639.5:c.-17_-16delinsTC ENSP00000451927.1:n.-17_-16delinsTC
NM_001312660.1:c.-17_-16delinsTC NP_001299589.1:n.-17_-16delinsTC
NM_001513.3:c.-17_-16delinsTC NP_001504.2:n.-17_-16delinsTC
NM_145870.2:c.149_150delinsTC NP_665877.1:p.Phe50=
NM_145871.2:c.149_150delinsTC NP_665878.2:p.Phe50=
XM_005267559.2:c.-17_-16delinsTC XP_005267616.1:n.-17_-16delinsTC
XM_011536670.1:c.-328_-327delinsTC XP_011534972.1:n.-328_-327delinsTC
XM_011536671.1:c.152_153delinsTC XP_011534973.1:p.Phe51=
NM_001363703.1:c.152_153delinsTC NP_001350632.1:p.Phe51=
XM_011536670.2:c.-328_-327delinsTC XP_011534972.1:n.-328_-327delinsTC
XM_011536671.2:c.152_153delinsTC XP_011534973.1:p.Phe51=
XM_024449549.1:c.-328_-327delinsTC XP_024305317.1:n.-328_-327delinsTC
XM_024449550.1:c.-17_-16delinsTC XP_024305318.1:n.-17_-16delinsTC
XM_024449551.1:c.-17_-16delinsTC XP_024305319.1:n.-17_-16delinsTC
XM_024449552.1:c.-17_-16delinsTC XP_024305320.1:n.-17_-16delinsTC
NM_145870.3:c.149_150delinsTC MANE Select NP_665877.1:p.Phe50=
NM_001312660.2:c.-17_-16delinsTC NP_001299589.1:n.-17_-16delinsTC
NM_001363703.2:c.152_153delinsTC NP_001350632.1:p.Phe51=
NM_145871.3:c.149_150delinsTC NP_665878.2:p.Phe50=