Canonical Allele Identifier: CA400711330

Gene: HELZ

Linked Data

• MyVariant Identifiers: chr17:g.65124895C>A (hg19) ; chr17:g.67128779C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67128779C>A , CM000679.2:g.67128779C>A	GRCh38
NC_000017.10:g.65124895C>A , CM000679.1:g.65124895C>A	GRCh37
NC_000017.9:g.62555357C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358691.10:c.3259G>T MANE Select	ENSP00000351524.5:p.Ala1087Ser
ENST00000358691.9:c.3259G>T	ENSP00000351524.5:p.Ala1087Ser
ENST00000579953.5:c.3262G>T	ENSP00000463727.1:p.Ala1088Ser
ENST00000580168.5:c.3262G>T	ENSP00000464512.1:p.Ala1088Ser
NM_014877.3:c.3259G>T	NP_055692.2:p.Ala1087Ser
XM_005257888.3:c.3340G>T	XP_005257945.1:p.Ala1114Ser
XM_005257889.3:c.3262G>T	XP_005257946.1:p.Ala1088Ser
XM_005257890.3:c.3238G>T	XP_005257947.1:p.Ala1080Ser
XM_006722214.2:c.3343G>T	XP_006722277.1:p.Ala1115Ser
XM_006722215.2:c.2638G>T	XP_006722278.1:p.Ala880Ser
XM_006722216.2:c.2167G>T	XP_006722279.1:p.Ala723Ser
XM_011525544.1:c.3343G>T	XP_011523846.1:p.Ala1115Ser
XM_011525545.1:c.3343G>T	XP_011523847.1:p.Ala1115Ser
XR_934629.1:n.3334G>T
NM_001330447.1:c.3262G>T	NP_001317376.1:p.Ala1088Ser
XM_005257888.5:c.3340G>T	XP_005257945.1:p.Ala1114Ser
XM_006722214.4:c.3343G>T	XP_006722277.1:p.Ala1115Ser
XM_006722215.3:c.2638G>T	XP_006722278.1:p.Ala880Ser
XM_006722216.3:c.2167G>T	XP_006722279.1:p.Ala723Ser
XM_011525544.2:c.3343G>T	XP_011523846.1:p.Ala1115Ser
XM_017025477.2:c.2554G>T	XP_016880966.1:p.Ala852Ser
XM_017025478.1:c.2086G>T	XP_016880967.1:p.Ala696Ser
XR_001752712.2:n.3434G>T
XR_001752713.2:n.3286G>T
XR_001752714.2:n.3202G>T
NM_014877.4:c.3259G>T MANE Select	NP_055692.3:p.Ala1087Ser
NM_001330447.2:c.3262G>T	NP_001317376.2:p.Ala1088Ser