Canonical Allele Identifier: CA501487665

Gene: HELZ

Linked Data

• MyVariant Identifiers: chr17:g.65124881A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67128765A>C , CM000679.2:g.67128765A>C	GRCh38
NC_000017.10:g.65124881A>C , CM000679.1:g.65124881A>C	GRCh37
NC_000017.9:g.62555343A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358691.10:c.3273T>G MANE Select	ENSP00000351524.5:p.Ala1091=
ENST00000358691.9:c.3273T>G	ENSP00000351524.5:p.Ala1091=
ENST00000579953.5:c.3276T>G	ENSP00000463727.1:p.Ala1092=
ENST00000580168.5:c.3276T>G	ENSP00000464512.1:p.Ala1092=
NM_014877.3:c.3273T>G	NP_055692.2:p.Ala1091=
XM_005257888.3:c.3354T>G	XP_005257945.1:p.Ala1118=
XM_005257889.3:c.3276T>G	XP_005257946.1:p.Ala1092=
XM_005257890.3:c.3252T>G	XP_005257947.1:p.Ala1084=
XM_006722214.2:c.3357T>G	XP_006722277.1:p.Ala1119=
XM_006722215.2:c.2652T>G	XP_006722278.1:p.Ala884=
XM_006722216.2:c.2181T>G	XP_006722279.1:p.Ala727=
XM_011525544.1:c.3357T>G	XP_011523846.1:p.Ala1119=
XM_011525545.1:c.3357T>G	XP_011523847.1:p.Ala1119=
XR_934629.1:n.3348T>G
NM_001330447.1:c.3276T>G	NP_001317376.1:p.Ala1092=
XM_005257888.5:c.3354T>G	XP_005257945.1:p.Ala1118=
XM_006722214.4:c.3357T>G	XP_006722277.1:p.Ala1119=
XM_006722215.3:c.2652T>G	XP_006722278.1:p.Ala884=
XM_006722216.3:c.2181T>G	XP_006722279.1:p.Ala727=
XM_011525544.2:c.3357T>G	XP_011523846.1:p.Ala1119=
XM_017025477.2:c.2568T>G	XP_016880966.1:p.Ala856=
XM_017025478.1:c.2100T>G	XP_016880967.1:p.Ala700=
XR_001752712.2:n.3448T>G
XR_001752713.2:n.3300T>G
XR_001752714.2:n.3216T>G
NM_014877.4:c.3273T>G MANE Select	NP_055692.3:p.Ala1091=
NM_001330447.2:c.3276T>G	NP_001317376.2:p.Ala1092=