Canonical Allele Identifier: CA2148346988

Gene: GSTZ1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77327168_77327169delinsGT , CM000676.2:g.77327168_77327169delinsGT	GRCh38
NC_000014.8:g.77793511_77793512delinsGT , CM000676.1:g.77793511_77793512delinsGT	GRCh37
NC_000014.7:g.76863264_76863265delinsGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216465.10:c.135+263_135+264delinsGT MANE Select	ENSP00000216465.5:n.135+263_135+264delinsGT
ENST00000216465.9:c.135+263_135+264delinsGT	ENSP00000216465.5:n.135+263_135+264delinsGT
ENST00000349555.7:c.135+263_135+264delinsGT	ENSP00000314404.5:n.135+263_135+264delinsGT
ENST00000361389.8:c.-31+263_-31+264delinsGT	ENSP00000354959.4:n.-31+263_-31+264delinsGT
ENST00000393734.5:c.-31+263_-31+264delinsGT	ENSP00000377335.1:n.-31+263_-31+264delinsGT
ENST00000553268.5:n.473_474delinsGT
ENST00000553431.5:n.266+263_266+264delinsGT
ENST00000553586.5:c.138+263_138+264delinsGT	ENSP00000451976.1:n.138+263_138+264delinsGT
ENST00000553838.5:n.305+263_305+264delinsGT
ENST00000554279.5:c.135+263_135+264delinsGT	ENSP00000452498.1:n.135+263_135+264delinsGT
ENST00000554846.5:c.-31+263_-31+264delinsGT	ENSP00000452531.1:n.-31+263_-31+264delinsGT
ENST00000555093.1:n.4184+263_4184+264delinsGT
ENST00000555583.1:c.-31+263_-31+264delinsGT	ENSP00000452346.1:n.-31+263_-31+264delinsGT
ENST00000556627.5:c.135+263_135+264delinsGT	ENSP00000450487.1:n.135+263_135+264delinsGT
ENST00000556914.5:n.215+263_215+264delinsGT
ENST00000557053.5:c.-31+263_-31+264delinsGT	ENSP00000451150.1:n.-31+263_-31+264delinsGT
ENST00000557639.5:c.-31+263_-31+264delinsGT	ENSP00000451927.1:n.-31+263_-31+264delinsGT
NM_001312660.1:c.-31+263_-31+264delinsGT	NP_001299589.1:n.-31+263_-31+264delinsGT
NM_001513.3:c.-31+263_-31+264delinsGT	NP_001504.2:n.-31+263_-31+264delinsGT
NM_145870.2:c.135+263_135+264delinsGT	NP_665877.1:n.135+263_135+264delinsGT
NM_145871.2:c.135+263_135+264delinsGT	NP_665878.2:n.135+263_135+264delinsGT
XM_005267559.2:c.-31+263_-31+264delinsGT	XP_005267616.1:n.-31+263_-31+264delinsGT
XM_011536670.1:c.-342+263_-342+264delinsGT	XP_011534972.1:n.-342+263_-342+264delinsGT
XM_011536671.1:c.138+263_138+264delinsGT	XP_011534973.1:n.138+263_138+264delinsGT
NM_001363703.1:c.138+263_138+264delinsGT	NP_001350632.1:n.138+263_138+264delinsGT
XM_011536670.2:c.-342+263_-342+264delinsGT	XP_011534972.1:n.-342+263_-342+264delinsGT
XM_011536671.2:c.138+263_138+264delinsGT	XP_011534973.1:n.138+263_138+264delinsGT
XM_024449549.1:c.-342+263_-342+264delinsGT	XP_024305317.1:n.-342+263_-342+264delinsGT
XM_024449550.1:c.-31+263_-31+264delinsGT	XP_024305318.1:n.-31+263_-31+264delinsGT
XM_024449551.1:c.-31+263_-31+264delinsGT	XP_024305319.1:n.-31+263_-31+264delinsGT
XM_024449552.1:c.-31+263_-31+264delinsGT	XP_024305320.1:n.-31+263_-31+264delinsGT
NM_145870.3:c.135+263_135+264delinsGT MANE Select	NP_665877.1:n.135+263_135+264delinsGT
NM_001312660.2:c.-31+263_-31+264delinsGT	NP_001299589.1:n.-31+263_-31+264delinsGT
NM_001363703.2:c.138+263_138+264delinsGT	NP_001350632.1:n.138+263_138+264delinsGT
NM_145871.3:c.135+263_135+264delinsGT	NP_665878.2:n.135+263_135+264delinsGT