Canonical Allele Identifier: CA2148347152

Gene: GSTZ1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77327540C= , CM000676.2:g.77327540C=	GRCh38
NC_000014.8:g.77793883C= , CM000676.1:g.77793883C=	GRCh37
NC_000014.7:g.76863636C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216465.10:c.204C= MANE Select	ENSP00000216465.5:p.Thr68=
ENST00000216465.9:c.204C=	ENSP00000216465.5:p.Thr68=
ENST00000349555.7:c.204C=	ENSP00000314404.5:p.Thr68=
ENST00000361389.8:c.39C=	ENSP00000354959.4:p.Thr13=
ENST00000393734.5:c.39C=	ENSP00000377335.1:p.Thr13=
ENST00000553431.5:n.335C=
ENST00000553586.5:c.207C=	ENSP00000451976.1:p.Thr69=
ENST00000553838.5:n.374C=
ENST00000554279.5:c.174+30C=	ENSP00000452498.1:n.174+30C=
ENST00000554846.5:c.39C=	ENSP00000452531.1:p.Thr13=
ENST00000555093.1:n.4253C=
ENST00000555583.1:c.39C=	ENSP00000452346.1:p.Thr13=
ENST00000556627.5:c.136-372C=	ENSP00000450487.1:n.136-372C=
ENST00000556914.5:n.284C=
ENST00000557053.5:c.39C=	ENSP00000451150.1:p.Thr13=
ENST00000557639.5:c.39C=	ENSP00000451927.1:p.Thr13=
NM_001312660.1:c.39C=	NP_001299589.1:p.Thr13=
NM_001513.3:c.39C=	NP_001504.2:p.Thr13=
NM_145870.2:c.204C=	NP_665877.1:p.Thr68=
NM_145871.2:c.204C=	NP_665878.2:p.Thr68=
XM_005267559.2:c.39C=	XP_005267616.1:p.Thr13=
XM_011536670.1:c.-273C=	XP_011534972.1:n.-273C=
XM_011536671.1:c.207C=	XP_011534973.1:p.Thr69=
NM_001363703.1:c.207C=	NP_001350632.1:p.Thr69=
XM_011536670.2:c.-273C=	XP_011534972.1:n.-273C=
XM_011536671.2:c.207C=	XP_011534973.1:p.Thr69=
XM_024449549.1:c.-273C=	XP_024305317.1:n.-273C=
XM_024449550.1:c.39C=	XP_024305318.1:p.Thr13=
XM_024449551.1:c.39C=	XP_024305319.1:p.Thr13=
XM_024449552.1:c.39C=	XP_024305320.1:p.Thr13=
NM_145870.3:c.204C= MANE Select	NP_665877.1:p.Thr68=
NM_001312660.2:c.39C=	NP_001299589.1:p.Thr13=
NM_001363703.2:c.207C=	NP_001350632.1:p.Thr69=
NM_145871.3:c.204C=	NP_665878.2:p.Thr68=