Canonical Allele Identifier: CA501487639

Gene: HELZ

Linked Data

• gnomAD v4: 17-67128740-A-G
• MyVariant Identifiers: chr17:g.65124856A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67128740A>G , CM000679.2:g.67128740A>G	GRCh38
NC_000017.10:g.65124856A>G , CM000679.1:g.65124856A>G	GRCh37
NC_000017.9:g.62555318A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358691.10:c.3298T>C MANE Select	ENSP00000351524.5:p.Leu1100=
ENST00000358691.9:c.3298T>C	ENSP00000351524.5:p.Leu1100=
ENST00000579953.5:c.3301T>C	ENSP00000463727.1:p.Leu1101=
ENST00000580168.5:c.3301T>C	ENSP00000464512.1:p.Leu1101=
NM_014877.3:c.3298T>C	NP_055692.2:p.Leu1100=
XM_005257888.3:c.3379T>C	XP_005257945.1:p.Leu1127=
XM_005257889.3:c.3301T>C	XP_005257946.1:p.Leu1101=
XM_005257890.3:c.3277T>C	XP_005257947.1:p.Leu1093=
XM_006722214.2:c.3382T>C	XP_006722277.1:p.Leu1128=
XM_006722215.2:c.2677T>C	XP_006722278.1:p.Leu893=
XM_006722216.2:c.2206T>C	XP_006722279.1:p.Leu736=
XM_011525544.1:c.3382T>C	XP_011523846.1:p.Leu1128=
XM_011525545.1:c.3382T>C	XP_011523847.1:p.Leu1128=
XR_934629.1:n.3373T>C
NM_001330447.1:c.3301T>C	NP_001317376.1:p.Leu1101=
XM_005257888.5:c.3379T>C	XP_005257945.1:p.Leu1127=
XM_006722214.4:c.3382T>C	XP_006722277.1:p.Leu1128=
XM_006722215.3:c.2677T>C	XP_006722278.1:p.Leu893=
XM_006722216.3:c.2206T>C	XP_006722279.1:p.Leu736=
XM_011525544.2:c.3382T>C	XP_011523846.1:p.Leu1128=
XM_017025477.2:c.2593T>C	XP_016880966.1:p.Leu865=
XM_017025478.1:c.2125T>C	XP_016880967.1:p.Leu709=
XR_001752712.2:n.3473T>C
XR_001752713.2:n.3325T>C
XR_001752714.2:n.3241T>C
NM_014877.4:c.3298T>C MANE Select	NP_055692.3:p.Leu1100=
NM_001330447.2:c.3301T>C	NP_001317376.2:p.Leu1101=