Canonical Allele Identifier: CA2148347148

Gene: GSTZ1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77327531_77327532delinsTG , CM000676.2:g.77327531_77327532delinsTG	GRCh38
NC_000014.8:g.77793874_77793875delinsTG , CM000676.1:g.77793874_77793875delinsTG	GRCh37
NC_000014.7:g.76863627_76863628delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216465.10:c.195_196delinsTG MANE Select	ENSP00000216465.5:p.Asp65=
ENST00000216465.9:c.195_196delinsTG	ENSP00000216465.5:p.Asp65=
ENST00000349555.7:c.195_196delinsTG	ENSP00000314404.5:p.Asp65=
ENST00000361389.8:c.30_31delinsTG	ENSP00000354959.4:p.Asp10=
ENST00000393734.5:c.30_31delinsTG	ENSP00000377335.1:p.Asp10=
ENST00000553431.5:n.326_327delinsTG
ENST00000553586.5:c.198_199delinsTG	ENSP00000451976.1:p.Asp66=
ENST00000553838.5:n.365_366delinsTG
ENST00000554279.5:c.174+21_174+22delinsTG	ENSP00000452498.1:n.174+21_174+22delinsTG
ENST00000554846.5:c.30_31delinsTG	ENSP00000452531.1:p.Asp10=
ENST00000555093.1:n.4244_4245delinsTG
ENST00000555583.1:c.30_31delinsTG	ENSP00000452346.1:p.Asp10=
ENST00000556627.5:c.136-381_136-380delinsTG	ENSP00000450487.1:n.136-381_136-380delinsTG
ENST00000556914.5:n.275_276delinsTG
ENST00000557053.5:c.30_31delinsTG	ENSP00000451150.1:p.Asp10=
ENST00000557639.5:c.30_31delinsTG	ENSP00000451927.1:p.Asp10=
NM_001312660.1:c.30_31delinsTG	NP_001299589.1:p.Asp10=
NM_001513.3:c.30_31delinsTG	NP_001504.2:p.Asp10=
NM_145870.2:c.195_196delinsTG	NP_665877.1:p.Asp65=
NM_145871.2:c.195_196delinsTG	NP_665878.2:p.Asp65=
XM_005267559.2:c.30_31delinsTG	XP_005267616.1:p.Asp10=
XM_011536670.1:c.-282_-281delinsTG	XP_011534972.1:n.-282_-281delinsTG
XM_011536671.1:c.198_199delinsTG	XP_011534973.1:p.Asp66=
NM_001363703.1:c.198_199delinsTG	NP_001350632.1:p.Asp66=
XM_011536670.2:c.-282_-281delinsTG	XP_011534972.1:n.-282_-281delinsTG
XM_011536671.2:c.198_199delinsTG	XP_011534973.1:p.Asp66=
XM_024449549.1:c.-282_-281delinsTG	XP_024305317.1:n.-282_-281delinsTG
XM_024449550.1:c.30_31delinsTG	XP_024305318.1:p.Asp10=
XM_024449551.1:c.30_31delinsTG	XP_024305319.1:p.Asp10=
XM_024449552.1:c.30_31delinsTG	XP_024305320.1:p.Asp10=
NM_145870.3:c.195_196delinsTG MANE Select	NP_665877.1:p.Asp65=
NM_001312660.2:c.30_31delinsTG	NP_001299589.1:p.Asp10=
NM_001363703.2:c.198_199delinsTG	NP_001350632.1:p.Asp66=
NM_145871.3:c.195_196delinsTG	NP_665878.2:p.Asp65=