Canonical Allele Identifier: CA487299723

Gene: GSTZ1

Linked Data

• MyVariant Identifiers: chr14:g.77793865G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77327522G>C , CM000676.2:g.77327522G>C	GRCh38
NC_000014.8:g.77793865G>C , CM000676.1:g.77793865G>C	GRCh37
NC_000014.7:g.76863618G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216465.10:c.186G>C MANE Select	ENSP00000216465.5:p.Leu62=
ENST00000216465.9:c.186G>C	ENSP00000216465.5:p.Leu62=
ENST00000349555.7:c.186G>C	ENSP00000314404.5:p.Leu62=
ENST00000361389.8:c.21G>C	ENSP00000354959.4:p.Leu7=
ENST00000393734.5:c.21G>C	ENSP00000377335.1:p.Leu7=
ENST00000553431.5:n.317G>C
ENST00000553586.5:c.189G>C	ENSP00000451976.1:p.Leu63=
ENST00000553838.5:n.356G>C
ENST00000554279.5:c.174+12G>C	ENSP00000452498.1:n.174+12G>C
ENST00000554846.5:c.21G>C	ENSP00000452531.1:p.Leu7=
ENST00000555093.1:n.4235G>C
ENST00000555583.1:c.21G>C	ENSP00000452346.1:p.Leu7=
ENST00000556627.5:c.136-390G>C	ENSP00000450487.1:n.136-390G>C
ENST00000556914.5:n.266G>C
ENST00000557053.5:c.21G>C	ENSP00000451150.1:p.Leu7=
ENST00000557639.5:c.21G>C	ENSP00000451927.1:p.Leu7=
NM_001312660.1:c.21G>C	NP_001299589.1:p.Leu7=
NM_001513.3:c.21G>C	NP_001504.2:p.Leu7=
NM_145870.2:c.186G>C	NP_665877.1:p.Leu62=
NM_145871.2:c.186G>C	NP_665878.2:p.Leu62=
XM_005267559.2:c.21G>C	XP_005267616.1:p.Leu7=
XM_011536670.1:c.-291G>C	XP_011534972.1:n.-291G>C
XM_011536671.1:c.189G>C	XP_011534973.1:p.Leu63=
NM_001363703.1:c.189G>C	NP_001350632.1:p.Leu63=
XM_011536670.2:c.-291G>C	XP_011534972.1:n.-291G>C
XM_011536671.2:c.189G>C	XP_011534973.1:p.Leu63=
XM_024449549.1:c.-291G>C	XP_024305317.1:n.-291G>C
XM_024449550.1:c.21G>C	XP_024305318.1:p.Leu7=
XM_024449551.1:c.21G>C	XP_024305319.1:p.Leu7=
XM_024449552.1:c.21G>C	XP_024305320.1:p.Leu7=
NM_145870.3:c.186G>C MANE Select	NP_665877.1:p.Leu62=
NM_001312660.2:c.21G>C	NP_001299589.1:p.Leu7=
NM_001363703.2:c.189G>C	NP_001350632.1:p.Leu63=
NM_145871.3:c.186G>C	NP_665878.2:p.Leu62=