Canonical Allele Identifier: CA358731776

Gene: NEK1

Linked Data

• gnomAD v4: 4-169508311-C-A
• MyVariant Identifiers: chr4:g.170429462C>A (hg19) ; chr4:g.169508311C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.169508311C>A , CM000666.2:g.169508311C>A	GRCh38
NC_000004.11:g.170429462C>A , CM000666.1:g.170429462C>A	GRCh37
NC_000004.10:g.170666037C>A	NCBI36
NG_027982.1:g.109317G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685111.1:c.1602G>T	ENSP00000508844.1:p.Arg534Ser
ENST00000685677.1:n.1068G>T
ENST00000686697.1:c.1560G>T	ENSP00000508689.1:p.Arg520Ser
ENST00000687054.1:n.2264G>T
ENST00000687219.1:c.*1273G>T	ENSP00000509736.1:n.*1273G>T
ENST00000687528.1:c.1638G>T	ENSP00000510228.1:p.Arg546Ser
ENST00000687643.1:c.1713G>T	ENSP00000509309.1:p.Arg571Ser
ENST00000688934.1:c.-112G>T	ENSP00000510760.1:n.-112G>T
ENST00000689190.1:n.1656G>T
ENST00000692450.1:c.*1435G>T	ENSP00000510283.1:n.*1435G>T
ENST00000693085.1:c.*1513G>T	ENSP00000508746.1:n.*1513G>T
ENST00000693604.1:c.*704G>T	ENSP00000509917.1:n.*704G>T
ENST00000507142.6:c.1770G>T MANE Select	ENSP00000424757.2:p.Arg590Ser
ENST00000439128.6:c.1686G>T	ENSP00000408020.2:p.Arg562Ser
ENST00000507142.5:c.1770G>T	ENSP00000424757.1:p.Arg590Ser
ENST00000510533.5:c.1554G>T	ENSP00000427653.1:p.Arg518Ser
ENST00000511633.5:c.1638G>T	ENSP00000423332.1:p.Arg546Ser
ENST00000512193.5:c.1479G>T	ENSP00000424938.1:p.Arg493Ser
NM_001199397.1:c.1770G>T	NP_001186326.1:p.Arg590Ser
NM_001199398.1:c.1638G>T	NP_001186327.1:p.Arg546Ser
NM_001199399.1:c.1479G>T	NP_001186328.1:p.Arg493Ser
NM_001199400.1:c.1554G>T	NP_001186329.1:p.Arg518Ser
NM_012224.2:c.1686G>T	NP_036356.1:p.Arg562Ser
XM_006714228.1:c.1770G>T	XP_006714291.1:p.Arg590Ser
XM_011532003.1:c.1686G>T	XP_011530305.1:p.Arg562Ser
XM_011532004.1:c.1554G>T	XP_011530306.1:p.Arg518Ser
XM_011532005.1:c.1770G>T	XP_011530307.1:p.Arg590Ser
XM_011532005.2:c.1770G>T	XP_011530307.1:p.Arg590Ser
XM_017008249.1:c.1149G>T	XP_016863738.1:p.Arg383Ser
XM_017008251.1:c.1065G>T	XP_016863740.1:p.Arg355Ser
XM_017008252.2:c.1065G>T	XP_016863741.1:p.Arg355Ser
XM_017008253.1:c.618G>T	XP_016863742.1:p.Arg206Ser
XM_017008254.1:c.414G>T	XP_016863743.1:p.Arg138Ser
XM_024454065.1:c.1149G>T	XP_024309833.1:p.Arg383Ser
XR_001741233.1:n.2350G>T
XR_001741234.2:n.2163G>T
NM_001199397.3:c.1770G>T MANE Select	NP_001186326.1:p.Arg590Ser
NM_001199398.2:c.1638G>T	NP_001186327.1:p.Arg546Ser
NM_001199399.2:c.1479G>T	NP_001186328.1:p.Arg493Ser
NM_001199400.2:c.1554G>T	NP_001186329.1:p.Arg518Ser
NM_001374418.1:c.1770G>T	NP_001361347.1:p.Arg590Ser
NM_001374419.1:c.1686G>T	NP_001361348.1:p.Arg562Ser
NM_001374420.1:c.1635G>T	NP_001361349.1:p.Arg545Ser
NM_001374421.1:c.1560G>T	NP_001361350.1:p.Arg520Ser
NM_012224.3:c.1686G>T	NP_036356.1:p.Arg562Ser
NR_164630.1:n.2232G>T
NM_001199398.3:c.1638G>T	NP_001186327.1:p.Arg546Ser
NM_001199399.3:c.1479G>T	NP_001186328.1:p.Arg493Ser
NM_001199400.3:c.1554G>T	NP_001186329.1:p.Arg518Ser
NM_012224.4:c.1686G>T	NP_036356.1:p.Arg562Ser