Canonical Allele Identifier: CA400711365

Gene: HELZ

Linked Data

• MyVariant Identifiers: chr17:g.65124909A>C (hg19) ; chr17:g.67128793A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67128793A>C , CM000679.2:g.67128793A>C	GRCh38
NC_000017.10:g.65124909A>C , CM000679.1:g.65124909A>C	GRCh37
NC_000017.9:g.62555371A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358691.10:c.3245T>G MANE Select	ENSP00000351524.5:p.Phe1082Cys
ENST00000358691.9:c.3245T>G	ENSP00000351524.5:p.Phe1082Cys
ENST00000579953.5:c.3248T>G	ENSP00000463727.1:p.Phe1083Cys
ENST00000580168.5:c.3248T>G	ENSP00000464512.1:p.Phe1083Cys
NM_014877.3:c.3245T>G	NP_055692.2:p.Phe1082Cys
XM_005257888.3:c.3326T>G	XP_005257945.1:p.Phe1109Cys
XM_005257889.3:c.3248T>G	XP_005257946.1:p.Phe1083Cys
XM_005257890.3:c.3224T>G	XP_005257947.1:p.Phe1075Cys
XM_006722214.2:c.3329T>G	XP_006722277.1:p.Phe1110Cys
XM_006722215.2:c.2624T>G	XP_006722278.1:p.Phe875Cys
XM_006722216.2:c.2153T>G	XP_006722279.1:p.Phe718Cys
XM_011525544.1:c.3329T>G	XP_011523846.1:p.Phe1110Cys
XM_011525545.1:c.3329T>G	XP_011523847.1:p.Phe1110Cys
XR_934629.1:n.3320T>G
NM_001330447.1:c.3248T>G	NP_001317376.1:p.Phe1083Cys
XM_005257888.5:c.3326T>G	XP_005257945.1:p.Phe1109Cys
XM_006722214.4:c.3329T>G	XP_006722277.1:p.Phe1110Cys
XM_006722215.3:c.2624T>G	XP_006722278.1:p.Phe875Cys
XM_006722216.3:c.2153T>G	XP_006722279.1:p.Phe718Cys
XM_011525544.2:c.3329T>G	XP_011523846.1:p.Phe1110Cys
XM_017025477.2:c.2540T>G	XP_016880966.1:p.Phe847Cys
XM_017025478.1:c.2072T>G	XP_016880967.1:p.Phe691Cys
XR_001752712.2:n.3420T>G
XR_001752713.2:n.3272T>G
XR_001752714.2:n.3188T>G
NM_014877.4:c.3245T>G MANE Select	NP_055692.3:p.Phe1082Cys
NM_001330447.2:c.3248T>G	NP_001317376.2:p.Phe1083Cys