Canonical Allele Identifier: CA400711297

Gene: HELZ

Linked Data

• MyVariant Identifiers: chr17:g.65124882G>T (hg19) ; chr17:g.67128766G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67128766G>T , CM000679.2:g.67128766G>T	GRCh38
NC_000017.10:g.65124882G>T , CM000679.1:g.65124882G>T	GRCh37
NC_000017.9:g.62555344G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358691.10:c.3272C>A MANE Select	ENSP00000351524.5:p.Ala1091Asp
ENST00000358691.9:c.3272C>A	ENSP00000351524.5:p.Ala1091Asp
ENST00000579953.5:c.3275C>A	ENSP00000463727.1:p.Ala1092Asp
ENST00000580168.5:c.3275C>A	ENSP00000464512.1:p.Ala1092Asp
NM_014877.3:c.3272C>A	NP_055692.2:p.Ala1091Asp
XM_005257888.3:c.3353C>A	XP_005257945.1:p.Ala1118Asp
XM_005257889.3:c.3275C>A	XP_005257946.1:p.Ala1092Asp
XM_005257890.3:c.3251C>A	XP_005257947.1:p.Ala1084Asp
XM_006722214.2:c.3356C>A	XP_006722277.1:p.Ala1119Asp
XM_006722215.2:c.2651C>A	XP_006722278.1:p.Ala884Asp
XM_006722216.2:c.2180C>A	XP_006722279.1:p.Ala727Asp
XM_011525544.1:c.3356C>A	XP_011523846.1:p.Ala1119Asp
XM_011525545.1:c.3356C>A	XP_011523847.1:p.Ala1119Asp
XR_934629.1:n.3347C>A
NM_001330447.1:c.3275C>A	NP_001317376.1:p.Ala1092Asp
XM_005257888.5:c.3353C>A	XP_005257945.1:p.Ala1118Asp
XM_006722214.4:c.3356C>A	XP_006722277.1:p.Ala1119Asp
XM_006722215.3:c.2651C>A	XP_006722278.1:p.Ala884Asp
XM_006722216.3:c.2180C>A	XP_006722279.1:p.Ala727Asp
XM_011525544.2:c.3356C>A	XP_011523846.1:p.Ala1119Asp
XM_017025477.2:c.2567C>A	XP_016880966.1:p.Ala856Asp
XM_017025478.1:c.2099C>A	XP_016880967.1:p.Ala700Asp
XR_001752712.2:n.3447C>A
XR_001752713.2:n.3299C>A
XR_001752714.2:n.3215C>A
NM_014877.4:c.3272C>A MANE Select	NP_055692.3:p.Ala1091Asp
NM_001330447.2:c.3275C>A	NP_001317376.2:p.Ala1092Asp