Canonical Allele Identifier: CA7286477

Gene: GSTZ1

Linked Data

• dbSNP Id: rs141800227
• ExAC: 14:77793870 T / C
• gnomAD v2: 14-77793870-T-C
• gnomAD v3: 14-77327527-T-C
• gnomAD v4: 14-77327527-T-C
• MyVariant Identifiers: chr14:g.77793870T>C (hg19) ; chr14:g.77327527T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77327527T>C , CM000676.2:g.77327527T>C	GRCh38
NC_000014.8:g.77793870T>C , CM000676.1:g.77793870T>C	GRCh37
NC_000014.7:g.76863623T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216465.10:c.191T>C MANE Select	ENSP00000216465.5:p.Ile64Thr
ENST00000216465.9:c.191T>C	ENSP00000216465.5:p.Ile64Thr
ENST00000349555.7:c.191T>C	ENSP00000314404.5:p.Ile64Thr
ENST00000361389.8:c.26T>C	ENSP00000354959.4:p.Ile9Thr
ENST00000393734.5:c.26T>C	ENSP00000377335.1:p.Ile9Thr
ENST00000553431.5:n.322T>C
ENST00000553586.5:c.194T>C	ENSP00000451976.1:p.Ile65Thr
ENST00000553838.5:n.361T>C
ENST00000554279.5:c.174+17T>C	ENSP00000452498.1:n.174+17T>C
ENST00000554846.5:c.26T>C	ENSP00000452531.1:p.Ile9Thr
ENST00000555093.1:n.4240T>C
ENST00000555583.1:c.26T>C	ENSP00000452346.1:p.Ile9Thr
ENST00000556627.5:c.136-385T>C	ENSP00000450487.1:n.136-385T>C
ENST00000556914.5:n.271T>C
ENST00000557053.5:c.26T>C	ENSP00000451150.1:p.Ile9Thr
ENST00000557639.5:c.26T>C	ENSP00000451927.1:p.Ile9Thr
NM_001312660.1:c.26T>C	NP_001299589.1:p.Ile9Thr
NM_001513.3:c.26T>C	NP_001504.2:p.Ile9Thr
NM_145870.2:c.191T>C	NP_665877.1:p.Ile64Thr
NM_145871.2:c.191T>C	NP_665878.2:p.Ile64Thr
XM_005267559.2:c.26T>C	XP_005267616.1:p.Ile9Thr
XM_011536670.1:c.-286T>C	XP_011534972.1:n.-286T>C
XM_011536671.1:c.194T>C	XP_011534973.1:p.Ile65Thr
NM_001363703.1:c.194T>C	NP_001350632.1:p.Ile65Thr
XM_011536670.2:c.-286T>C	XP_011534972.1:n.-286T>C
XM_011536671.2:c.194T>C	XP_011534973.1:p.Ile65Thr
XM_024449549.1:c.-286T>C	XP_024305317.1:n.-286T>C
XM_024449550.1:c.26T>C	XP_024305318.1:p.Ile9Thr
XM_024449551.1:c.26T>C	XP_024305319.1:p.Ile9Thr
XM_024449552.1:c.26T>C	XP_024305320.1:p.Ile9Thr
NM_145870.3:c.191T>C MANE Select	NP_665877.1:p.Ile64Thr
NM_001312660.2:c.26T>C	NP_001299589.1:p.Ile9Thr
NM_001363703.2:c.194T>C	NP_001350632.1:p.Ile65Thr
NM_145871.3:c.191T>C	NP_665878.2:p.Ile64Thr