Canonical Allele Identifier: CA487299746

Gene: GSTZ1

Linked Data

• gnomAD v4: 14-77327528-T-A
• MyVariant Identifiers: chr14:g.77793871T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77327528T>A , CM000676.2:g.77327528T>A	GRCh38
NC_000014.8:g.77793871T>A , CM000676.1:g.77793871T>A	GRCh37
NC_000014.7:g.76863624T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216465.10:c.192T>A MANE Select	ENSP00000216465.5:p.Ile64=
ENST00000216465.9:c.192T>A	ENSP00000216465.5:p.Ile64=
ENST00000349555.7:c.192T>A	ENSP00000314404.5:p.Ile64=
ENST00000361389.8:c.27T>A	ENSP00000354959.4:p.Ile9=
ENST00000393734.5:c.27T>A	ENSP00000377335.1:p.Ile9=
ENST00000553431.5:n.323T>A
ENST00000553586.5:c.195T>A	ENSP00000451976.1:p.Ile65=
ENST00000553838.5:n.362T>A
ENST00000554279.5:c.174+18T>A	ENSP00000452498.1:n.174+18T>A
ENST00000554846.5:c.27T>A	ENSP00000452531.1:p.Ile9=
ENST00000555093.1:n.4241T>A
ENST00000555583.1:c.27T>A	ENSP00000452346.1:p.Ile9=
ENST00000556627.5:c.136-384T>A	ENSP00000450487.1:n.136-384T>A
ENST00000556914.5:n.272T>A
ENST00000557053.5:c.27T>A	ENSP00000451150.1:p.Ile9=
ENST00000557639.5:c.27T>A	ENSP00000451927.1:p.Ile9=
NM_001312660.1:c.27T>A	NP_001299589.1:p.Ile9=
NM_001513.3:c.27T>A	NP_001504.2:p.Ile9=
NM_145870.2:c.192T>A	NP_665877.1:p.Ile64=
NM_145871.2:c.192T>A	NP_665878.2:p.Ile64=
XM_005267559.2:c.27T>A	XP_005267616.1:p.Ile9=
XM_011536670.1:c.-285T>A	XP_011534972.1:n.-285T>A
XM_011536671.1:c.195T>A	XP_011534973.1:p.Ile65=
NM_001363703.1:c.195T>A	NP_001350632.1:p.Ile65=
XM_011536670.2:c.-285T>A	XP_011534972.1:n.-285T>A
XM_011536671.2:c.195T>A	XP_011534973.1:p.Ile65=
XM_024449549.1:c.-285T>A	XP_024305317.1:n.-285T>A
XM_024449550.1:c.27T>A	XP_024305318.1:p.Ile9=
XM_024449551.1:c.27T>A	XP_024305319.1:p.Ile9=
XM_024449552.1:c.27T>A	XP_024305320.1:p.Ile9=
NM_145870.3:c.192T>A MANE Select	NP_665877.1:p.Ile64=
NM_001312660.2:c.27T>A	NP_001299589.1:p.Ile9=
NM_001363703.2:c.195T>A	NP_001350632.1:p.Ile65=
NM_145871.3:c.192T>A	NP_665878.2:p.Ile64=