Canonical Allele Identifier: CA400711322

Gene: HELZ

Linked Data

• MyVariant Identifiers: chr17:g.65124891T>G (hg19) ; chr17:g.67128775T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67128775T>G , CM000679.2:g.67128775T>G	GRCh38
NC_000017.10:g.65124891T>G , CM000679.1:g.65124891T>G	GRCh37
NC_000017.9:g.62555353T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358691.10:c.3263A>C MANE Select	ENSP00000351524.5:p.Gln1088Pro
ENST00000358691.9:c.3263A>C	ENSP00000351524.5:p.Gln1088Pro
ENST00000579953.5:c.3266A>C	ENSP00000463727.1:p.Gln1089Pro
ENST00000580168.5:c.3266A>C	ENSP00000464512.1:p.Gln1089Pro
NM_014877.3:c.3263A>C	NP_055692.2:p.Gln1088Pro
XM_005257888.3:c.3344A>C	XP_005257945.1:p.Gln1115Pro
XM_005257889.3:c.3266A>C	XP_005257946.1:p.Gln1089Pro
XM_005257890.3:c.3242A>C	XP_005257947.1:p.Gln1081Pro
XM_006722214.2:c.3347A>C	XP_006722277.1:p.Gln1116Pro
XM_006722215.2:c.2642A>C	XP_006722278.1:p.Gln881Pro
XM_006722216.2:c.2171A>C	XP_006722279.1:p.Gln724Pro
XM_011525544.1:c.3347A>C	XP_011523846.1:p.Gln1116Pro
XM_011525545.1:c.3347A>C	XP_011523847.1:p.Gln1116Pro
XR_934629.1:n.3338A>C
NM_001330447.1:c.3266A>C	NP_001317376.1:p.Gln1089Pro
XM_005257888.5:c.3344A>C	XP_005257945.1:p.Gln1115Pro
XM_006722214.4:c.3347A>C	XP_006722277.1:p.Gln1116Pro
XM_006722215.3:c.2642A>C	XP_006722278.1:p.Gln881Pro
XM_006722216.3:c.2171A>C	XP_006722279.1:p.Gln724Pro
XM_011525544.2:c.3347A>C	XP_011523846.1:p.Gln1116Pro
XM_017025477.2:c.2558A>C	XP_016880966.1:p.Gln853Pro
XM_017025478.1:c.2090A>C	XP_016880967.1:p.Gln697Pro
XR_001752712.2:n.3438A>C
XR_001752713.2:n.3290A>C
XR_001752714.2:n.3206A>C
NM_014877.4:c.3263A>C MANE Select	NP_055692.3:p.Gln1088Pro
NM_001330447.2:c.3266A>C	NP_001317376.2:p.Gln1089Pro