Canonical Allele Identifier: CA2271598009

Gene: HELZ

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67128759T= , CM000679.2:g.67128759T=	GRCh38
NC_000017.10:g.65124875T= , CM000679.1:g.65124875T=	GRCh37
NC_000017.9:g.62555337T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358691.10:c.3279A= MANE Select	ENSP00000351524.5:p.Glu1093=
ENST00000358691.9:c.3279A=	ENSP00000351524.5:p.Glu1093=
ENST00000579953.5:c.3282A=	ENSP00000463727.1:p.Glu1094=
ENST00000580168.5:c.3282A=	ENSP00000464512.1:p.Glu1094=
NM_014877.3:c.3279A=	NP_055692.2:p.Glu1093=
XM_005257888.3:c.3360A=	XP_005257945.1:p.Glu1120=
XM_005257889.3:c.3282A=	XP_005257946.1:p.Glu1094=
XM_005257890.3:c.3258A=	XP_005257947.1:p.Glu1086=
XM_006722214.2:c.3363A=	XP_006722277.1:p.Glu1121=
XM_006722215.2:c.2658A=	XP_006722278.1:p.Glu886=
XM_006722216.2:c.2187A=	XP_006722279.1:p.Glu729=
XM_011525544.1:c.3363A=	XP_011523846.1:p.Glu1121=
XM_011525545.1:c.3363A=	XP_011523847.1:p.Glu1121=
XR_934629.1:n.3354A=
NM_001330447.1:c.3282A=	NP_001317376.1:p.Glu1094=
XM_005257888.5:c.3360A=	XP_005257945.1:p.Glu1120=
XM_006722214.4:c.3363A=	XP_006722277.1:p.Glu1121=
XM_006722215.3:c.2658A=	XP_006722278.1:p.Glu886=
XM_006722216.3:c.2187A=	XP_006722279.1:p.Glu729=
XM_011525544.2:c.3363A=	XP_011523846.1:p.Glu1121=
XM_017025477.2:c.2574A=	XP_016880966.1:p.Glu858=
XM_017025478.1:c.2106A=	XP_016880967.1:p.Glu702=
XR_001752712.2:n.3454A=
XR_001752713.2:n.3306A=
XR_001752714.2:n.3222A=
NM_014877.4:c.3279A= MANE Select	NP_055692.3:p.Glu1093=
NM_001330447.2:c.3282A=	NP_001317376.2:p.Glu1094=