Canonical Allele Identifier: CA501487698

Gene: HELZ

Linked Data

• COSMIC: COSM6035694
• MyVariant Identifiers: chr17:g.65124926G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67128810G>A , CM000679.2:g.67128810G>A	GRCh38
NC_000017.10:g.65124926G>A , CM000679.1:g.65124926G>A	GRCh37
NC_000017.9:g.62555388G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358691.10:c.3228C>T MANE Select	ENSP00000351524.5:p.Ser1076=
ENST00000358691.9:c.3228C>T	ENSP00000351524.5:p.Ser1076=
ENST00000579953.5:c.3231C>T	ENSP00000463727.1:p.Ser1077=
ENST00000580168.5:c.3231C>T	ENSP00000464512.1:p.Ser1077=
NM_014877.3:c.3228C>T	NP_055692.2:p.Ser1076=
XM_005257888.3:c.3309C>T	XP_005257945.1:p.Ser1103=
XM_005257889.3:c.3231C>T	XP_005257946.1:p.Ser1077=
XM_005257890.3:c.3207C>T	XP_005257947.1:p.Ser1069=
XM_006722214.2:c.3312C>T	XP_006722277.1:p.Ser1104=
XM_006722215.2:c.2607C>T	XP_006722278.1:p.Ser869=
XM_006722216.2:c.2136C>T	XP_006722279.1:p.Ser712=
XM_011525544.1:c.3312C>T	XP_011523846.1:p.Ser1104=
XM_011525545.1:c.3312C>T	XP_011523847.1:p.Ser1104=
XR_934629.1:n.3303C>T
NM_001330447.1:c.3231C>T	NP_001317376.1:p.Ser1077=
XM_005257888.5:c.3309C>T	XP_005257945.1:p.Ser1103=
XM_006722214.4:c.3312C>T	XP_006722277.1:p.Ser1104=
XM_006722215.3:c.2607C>T	XP_006722278.1:p.Ser869=
XM_006722216.3:c.2136C>T	XP_006722279.1:p.Ser712=
XM_011525544.2:c.3312C>T	XP_011523846.1:p.Ser1104=
XM_017025477.2:c.2523C>T	XP_016880966.1:p.Ser841=
XM_017025478.1:c.2055C>T	XP_016880967.1:p.Ser685=
XR_001752712.2:n.3403C>T
XR_001752713.2:n.3255C>T
XR_001752714.2:n.3171C>T
NM_014877.4:c.3228C>T MANE Select	NP_055692.3:p.Ser1076=
NM_001330447.2:c.3231C>T	NP_001317376.2:p.Ser1077=