Canonical Allele Identifier: CA263799087

Gene: GSTZ1

Linked Data

• dbSNP Id: rs1004329398
• gnomAD v3: 14-77327525-GATTGATGGA-G
• gnomAD v4: 14-77327525-GATTGATGGA-G
• MyVariant Identifiers: chr14:g.77793869_77793877del (hg19) ; chr14:g.77327526_77327534del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77327528_77327536del , CM000676.2:g.77327528_77327536del	GRCh38
NC_000014.8:g.77793871_77793879del , CM000676.1:g.77793871_77793879del	GRCh37
NC_000014.7:g.76863624_76863632del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216465.10:c.192_200del MANE Select	ENSP00000216465.5:p.Asp65_Ile67del
ENST00000216465.9:c.192_200del	ENSP00000216465.5:p.Asp65_Ile67del
ENST00000349555.7:c.192_200del	ENSP00000314404.5:p.Asp65_Ile67del
ENST00000361389.8:c.27_35del	ENSP00000354959.4:p.Asp10_Ile12del
ENST00000393734.5:c.27_35del	ENSP00000377335.1:p.Asp10_Ile12del
ENST00000553431.5:n.323_331del
ENST00000553586.5:c.195_203del	ENSP00000451976.1:p.Asp66_Ile68del
ENST00000553838.5:n.362_370del
ENST00000554279.5:c.174+18_174+26del	ENSP00000452498.1:n.174+18_174+26del
ENST00000554846.5:c.27_35del	ENSP00000452531.1:p.Asp10_Ile12del
ENST00000555093.1:n.4241_4249del
ENST00000555583.1:c.27_35del	ENSP00000452346.1:p.Asp10_Ile12del
ENST00000556627.5:c.136-384_136-376del	ENSP00000450487.1:n.136-384_136-376del
ENST00000556914.5:n.272_280del
ENST00000557053.5:c.27_35del	ENSP00000451150.1:p.Asp10_Ile12del
ENST00000557639.5:c.27_35del	ENSP00000451927.1:p.Asp10_Ile12del
NM_001312660.1:c.27_35del	NP_001299589.1:p.Asp10_Ile12del
NM_001513.3:c.27_35del	NP_001504.2:p.Asp10_Ile12del
NM_145870.2:c.192_200del	NP_665877.1:p.Asp65_Ile67del
NM_145871.2:c.192_200del	NP_665878.2:p.Asp65_Ile67del
XM_005267559.2:c.27_35del	XP_005267616.1:p.Asp10_Ile12del
XM_011536670.1:c.-285_-277del	XP_011534972.1:n.-285_-277del
XM_011536671.1:c.195_203del	XP_011534973.1:p.Asp66_Ile68del
NM_001363703.1:c.195_203del	NP_001350632.1:p.Asp66_Ile68del
XM_011536670.2:c.-285_-277del	XP_011534972.1:n.-285_-277del
XM_011536671.2:c.195_203del	XP_011534973.1:p.Asp66_Ile68del
XM_024449549.1:c.-285_-277del	XP_024305317.1:n.-285_-277del
XM_024449550.1:c.27_35del	XP_024305318.1:p.Asp10_Ile12del
XM_024449551.1:c.27_35del	XP_024305319.1:p.Asp10_Ile12del
XM_024449552.1:c.27_35del	XP_024305320.1:p.Asp10_Ile12del
NM_145870.3:c.192_200del MANE Select	NP_665877.1:p.Asp65_Ile67del
NM_001312660.2:c.27_35del	NP_001299589.1:p.Asp10_Ile12del
NM_001363703.2:c.195_203del	NP_001350632.1:p.Asp66_Ile68del
NM_145871.3:c.192_200del	NP_665878.2:p.Asp65_Ile67del