Canonical Allele Identifier: CA2271598015

Gene: HELZ

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67128788G= , CM000679.2:g.67128788G=	GRCh38
NC_000017.10:g.65124904G= , CM000679.1:g.65124904G=	GRCh37
NC_000017.9:g.62555366G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358691.10:c.3250C= MANE Select	ENSP00000351524.5:p.Gln1084=
ENST00000358691.9:c.3250C=	ENSP00000351524.5:p.Gln1084=
ENST00000579953.5:c.3253C=	ENSP00000463727.1:p.Gln1085=
ENST00000580168.5:c.3253C=	ENSP00000464512.1:p.Gln1085=
NM_014877.3:c.3250C=	NP_055692.2:p.Gln1084=
XM_005257888.3:c.3331C=	XP_005257945.1:p.Gln1111=
XM_005257889.3:c.3253C=	XP_005257946.1:p.Gln1085=
XM_005257890.3:c.3229C=	XP_005257947.1:p.Gln1077=
XM_006722214.2:c.3334C=	XP_006722277.1:p.Gln1112=
XM_006722215.2:c.2629C=	XP_006722278.1:p.Gln877=
XM_006722216.2:c.2158C=	XP_006722279.1:p.Gln720=
XM_011525544.1:c.3334C=	XP_011523846.1:p.Gln1112=
XM_011525545.1:c.3334C=	XP_011523847.1:p.Gln1112=
XR_934629.1:n.3325C=
NM_001330447.1:c.3253C=	NP_001317376.1:p.Gln1085=
XM_005257888.5:c.3331C=	XP_005257945.1:p.Gln1111=
XM_006722214.4:c.3334C=	XP_006722277.1:p.Gln1112=
XM_006722215.3:c.2629C=	XP_006722278.1:p.Gln877=
XM_006722216.3:c.2158C=	XP_006722279.1:p.Gln720=
XM_011525544.2:c.3334C=	XP_011523846.1:p.Gln1112=
XM_017025477.2:c.2545C=	XP_016880966.1:p.Gln849=
XM_017025478.1:c.2077C=	XP_016880967.1:p.Gln693=
XR_001752712.2:n.3425C=
XR_001752713.2:n.3277C=
XR_001752714.2:n.3193C=
NM_014877.4:c.3250C= MANE Select	NP_055692.3:p.Gln1084=
NM_001330447.2:c.3253C=	NP_001317376.2:p.Gln1085=