Canonical Allele Identifier: CA7286466

Gene: GSTZ1

Linked Data

• dbSNP Id: rs752382535
• ExAC: 14:77793809 CCA / C
• gnomAD v2: 14-77793809-CCA-C
• gnomAD v3: 14-77327466-CCA-C
• gnomAD v4: 14-77327466-CCA-C
• MyVariant Identifiers: chr14:g.77793810_77793811del (hg19) ; chr14:g.77327467_77327468del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77327469_77327470del , CM000676.2:g.77327469_77327470del	GRCh38
NC_000014.8:g.77793812_77793813del , CM000676.1:g.77793812_77793813del	GRCh37
NC_000014.7:g.76863565_76863566del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216465.10:c.136-3_136-2del MANE Select	ENSP00000216465.5:n.136-3_136-2del
ENST00000216465.9:c.136-3_136-2del	ENSP00000216465.5:n.136-3_136-2del
ENST00000349555.7:c.136-3_136-2del	ENSP00000314404.5:n.136-3_136-2del
ENST00000361389.8:c.-30-3_-30-2del	ENSP00000354959.4:n.-30-3_-30-2del
ENST00000393734.5:c.-30-3_-30-2del	ENSP00000377335.1:n.-30-3_-30-2del
ENST00000553431.5:n.267-3_267-2del
ENST00000553586.5:c.139-3_139-2del	ENSP00000451976.1:n.139-3_139-2del
ENST00000553838.5:n.306-3_306-2del
ENST00000554279.5:c.136-3_136-2del	ENSP00000452498.1:n.136-3_136-2del
ENST00000554846.5:c.-30-3_-30-2del	ENSP00000452531.1:n.-30-3_-30-2del
ENST00000555093.1:n.4185-3_4185-2del
ENST00000555583.1:c.-30-3_-30-2del	ENSP00000452346.1:n.-30-3_-30-2del
ENST00000556627.5:c.136-443_136-442del	ENSP00000450487.1:n.136-443_136-442del
ENST00000556914.5:n.216-3_216-2del
ENST00000557053.5:c.-30-3_-30-2del	ENSP00000451150.1:n.-30-3_-30-2del
ENST00000557639.5:c.-30-3_-30-2del	ENSP00000451927.1:n.-30-3_-30-2del
NM_001312660.1:c.-30-3_-30-2del	NP_001299589.1:n.-30-3_-30-2del
NM_001513.3:c.-30-3_-30-2del	NP_001504.2:n.-30-3_-30-2del
NM_145870.2:c.136-3_136-2del	NP_665877.1:n.136-3_136-2del
NM_145871.2:c.136-3_136-2del	NP_665878.2:n.136-3_136-2del
XM_005267559.2:c.-30-3_-30-2del	XP_005267616.1:n.-30-3_-30-2del
XM_011536670.1:c.-341-3_-341-2del	XP_011534972.1:n.-341-3_-341-2del
XM_011536671.1:c.139-3_139-2del	XP_011534973.1:n.139-3_139-2del
NM_001363703.1:c.139-3_139-2del	NP_001350632.1:n.139-3_139-2del
XM_011536670.2:c.-341-3_-341-2del	XP_011534972.1:n.-341-3_-341-2del
XM_011536671.2:c.139-3_139-2del	XP_011534973.1:n.139-3_139-2del
XM_024449549.1:c.-341-3_-341-2del	XP_024305317.1:n.-341-3_-341-2del
XM_024449550.1:c.-30-3_-30-2del	XP_024305318.1:n.-30-3_-30-2del
XM_024449551.1:c.-30-3_-30-2del	XP_024305319.1:n.-30-3_-30-2del
XM_024449552.1:c.-30-3_-30-2del	XP_024305320.1:n.-30-3_-30-2del
NM_145870.3:c.136-3_136-2del MANE Select	NP_665877.1:n.136-3_136-2del
NM_001312660.2:c.-30-3_-30-2del	NP_001299589.1:n.-30-3_-30-2del
NM_001363703.2:c.139-3_139-2del	NP_001350632.1:n.139-3_139-2del
NM_145871.3:c.136-3_136-2del	NP_665878.2:n.136-3_136-2del