Canonical Allele Identifier: CA400711301

Gene: HELZ

Linked Data

• MyVariant Identifiers: chr17:g.65124883C>G (hg19) ; chr17:g.67128767C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67128767C>G , CM000679.2:g.67128767C>G	GRCh38
NC_000017.10:g.65124883C>G , CM000679.1:g.65124883C>G	GRCh37
NC_000017.9:g.62555345C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358691.10:c.3271G>C MANE Select	ENSP00000351524.5:p.Ala1091Pro
ENST00000358691.9:c.3271G>C	ENSP00000351524.5:p.Ala1091Pro
ENST00000579953.5:c.3274G>C	ENSP00000463727.1:p.Ala1092Pro
ENST00000580168.5:c.3274G>C	ENSP00000464512.1:p.Ala1092Pro
NM_014877.3:c.3271G>C	NP_055692.2:p.Ala1091Pro
XM_005257888.3:c.3352G>C	XP_005257945.1:p.Ala1118Pro
XM_005257889.3:c.3274G>C	XP_005257946.1:p.Ala1092Pro
XM_005257890.3:c.3250G>C	XP_005257947.1:p.Ala1084Pro
XM_006722214.2:c.3355G>C	XP_006722277.1:p.Ala1119Pro
XM_006722215.2:c.2650G>C	XP_006722278.1:p.Ala884Pro
XM_006722216.2:c.2179G>C	XP_006722279.1:p.Ala727Pro
XM_011525544.1:c.3355G>C	XP_011523846.1:p.Ala1119Pro
XM_011525545.1:c.3355G>C	XP_011523847.1:p.Ala1119Pro
XR_934629.1:n.3346G>C
NM_001330447.1:c.3274G>C	NP_001317376.1:p.Ala1092Pro
XM_005257888.5:c.3352G>C	XP_005257945.1:p.Ala1118Pro
XM_006722214.4:c.3355G>C	XP_006722277.1:p.Ala1119Pro
XM_006722215.3:c.2650G>C	XP_006722278.1:p.Ala884Pro
XM_006722216.3:c.2179G>C	XP_006722279.1:p.Ala727Pro
XM_011525544.2:c.3355G>C	XP_011523846.1:p.Ala1119Pro
XM_017025477.2:c.2566G>C	XP_016880966.1:p.Ala856Pro
XM_017025478.1:c.2098G>C	XP_016880967.1:p.Ala700Pro
XR_001752712.2:n.3446G>C
XR_001752713.2:n.3298G>C
XR_001752714.2:n.3214G>C
NM_014877.4:c.3271G>C MANE Select	NP_055692.3:p.Ala1091Pro
NM_001330447.2:c.3274G>C	NP_001317376.2:p.Ala1092Pro