Canonical Allele Identifier: CA390507590

Gene: GSTZ1

Linked Data

• MyVariant Identifiers: chr14:g.77793861C>T (hg19) ; chr14:g.77327518C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77327518C>T , CM000676.2:g.77327518C>T	GRCh38
NC_000014.8:g.77793861C>T , CM000676.1:g.77793861C>T	GRCh37
NC_000014.7:g.76863614C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216465.10:c.182C>T MANE Select	ENSP00000216465.5:p.Thr61Ile
ENST00000216465.9:c.182C>T	ENSP00000216465.5:p.Thr61Ile
ENST00000349555.7:c.182C>T	ENSP00000314404.5:p.Thr61Ile
ENST00000361389.8:c.17C>T	ENSP00000354959.4:p.Thr6Ile
ENST00000393734.5:c.17C>T	ENSP00000377335.1:p.Thr6Ile
ENST00000553431.5:n.313C>T
ENST00000553586.5:c.185C>T	ENSP00000451976.1:p.Thr62Ile
ENST00000553838.5:n.352C>T
ENST00000554279.5:c.174+8C>T	ENSP00000452498.1:n.174+8C>T
ENST00000554846.5:c.17C>T	ENSP00000452531.1:p.Thr6Ile
ENST00000555093.1:n.4231C>T
ENST00000555583.1:c.17C>T	ENSP00000452346.1:p.Thr6Ile
ENST00000556627.5:c.136-394C>T	ENSP00000450487.1:n.136-394C>T
ENST00000556914.5:n.262C>T
ENST00000557053.5:c.17C>T	ENSP00000451150.1:p.Thr6Ile
ENST00000557639.5:c.17C>T	ENSP00000451927.1:p.Thr6Ile
NM_001312660.1:c.17C>T	NP_001299589.1:p.Thr6Ile
NM_001513.3:c.17C>T	NP_001504.2:p.Thr6Ile
NM_145870.2:c.182C>T	NP_665877.1:p.Thr61Ile
NM_145871.2:c.182C>T	NP_665878.2:p.Thr61Ile
XM_005267559.2:c.17C>T	XP_005267616.1:p.Thr6Ile
XM_011536670.1:c.-295C>T	XP_011534972.1:n.-295C>T
XM_011536671.1:c.185C>T	XP_011534973.1:p.Thr62Ile
NM_001363703.1:c.185C>T	NP_001350632.1:p.Thr62Ile
XM_011536670.2:c.-295C>T	XP_011534972.1:n.-295C>T
XM_011536671.2:c.185C>T	XP_011534973.1:p.Thr62Ile
XM_024449549.1:c.-295C>T	XP_024305317.1:n.-295C>T
XM_024449550.1:c.17C>T	XP_024305318.1:p.Thr6Ile
XM_024449551.1:c.17C>T	XP_024305319.1:p.Thr6Ile
XM_024449552.1:c.17C>T	XP_024305320.1:p.Thr6Ile
NM_145870.3:c.182C>T MANE Select	NP_665877.1:p.Thr61Ile
NM_001312660.2:c.17C>T	NP_001299589.1:p.Thr6Ile
NM_001363703.2:c.185C>T	NP_001350632.1:p.Thr62Ile
NM_145871.3:c.182C>T	NP_665878.2:p.Thr61Ile