Canonical Allele Identifier: CA358731781

Gene: NEK1

Linked Data

• gnomAD v4: 4-169508313-T-A
• MyVariant Identifiers: chr4:g.170429464T>A (hg19) ; chr4:g.169508313T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.169508313T>A , CM000666.2:g.169508313T>A	GRCh38
NC_000004.11:g.170429464T>A , CM000666.1:g.170429464T>A	GRCh37
NC_000004.10:g.170666039T>A	NCBI36
NG_027982.1:g.109315A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685111.1:c.1600A>T	ENSP00000508844.1:p.Arg534Trp
ENST00000685677.1:n.1066A>T
ENST00000686697.1:c.1558A>T	ENSP00000508689.1:p.Arg520Trp
ENST00000687054.1:n.2262A>T
ENST00000687219.1:c.*1271A>T	ENSP00000509736.1:n.*1271A>T
ENST00000687528.1:c.1636A>T	ENSP00000510228.1:p.Arg546Trp
ENST00000687643.1:c.1711A>T	ENSP00000509309.1:p.Arg571Trp
ENST00000688934.1:c.-114A>T	ENSP00000510760.1:n.-114A>T
ENST00000689190.1:n.1654A>T
ENST00000692450.1:c.*1433A>T	ENSP00000510283.1:n.*1433A>T
ENST00000693085.1:c.*1511A>T	ENSP00000508746.1:n.*1511A>T
ENST00000693604.1:c.*702A>T	ENSP00000509917.1:n.*702A>T
ENST00000507142.6:c.1768A>T MANE Select	ENSP00000424757.2:p.Arg590Trp
ENST00000439128.6:c.1684A>T	ENSP00000408020.2:p.Arg562Trp
ENST00000507142.5:c.1768A>T	ENSP00000424757.1:p.Arg590Trp
ENST00000510533.5:c.1552A>T	ENSP00000427653.1:p.Arg518Trp
ENST00000511633.5:c.1636A>T	ENSP00000423332.1:p.Arg546Trp
ENST00000512193.5:c.1477A>T	ENSP00000424938.1:p.Arg493Trp
NM_001199397.1:c.1768A>T	NP_001186326.1:p.Arg590Trp
NM_001199398.1:c.1636A>T	NP_001186327.1:p.Arg546Trp
NM_001199399.1:c.1477A>T	NP_001186328.1:p.Arg493Trp
NM_001199400.1:c.1552A>T	NP_001186329.1:p.Arg518Trp
NM_012224.2:c.1684A>T	NP_036356.1:p.Arg562Trp
XM_006714228.1:c.1768A>T	XP_006714291.1:p.Arg590Trp
XM_011532003.1:c.1684A>T	XP_011530305.1:p.Arg562Trp
XM_011532004.1:c.1552A>T	XP_011530306.1:p.Arg518Trp
XM_011532005.1:c.1768A>T	XP_011530307.1:p.Arg590Trp
XM_011532005.2:c.1768A>T	XP_011530307.1:p.Arg590Trp
XM_017008249.1:c.1147A>T	XP_016863738.1:p.Arg383Trp
XM_017008251.1:c.1063A>T	XP_016863740.1:p.Arg355Trp
XM_017008252.2:c.1063A>T	XP_016863741.1:p.Arg355Trp
XM_017008253.1:c.616A>T	XP_016863742.1:p.Arg206Trp
XM_017008254.1:c.412A>T	XP_016863743.1:p.Arg138Trp
XM_024454065.1:c.1147A>T	XP_024309833.1:p.Arg383Trp
XR_001741233.1:n.2348A>T
XR_001741234.2:n.2161A>T
NM_001199397.3:c.1768A>T MANE Select	NP_001186326.1:p.Arg590Trp
NM_001199398.2:c.1636A>T	NP_001186327.1:p.Arg546Trp
NM_001199399.2:c.1477A>T	NP_001186328.1:p.Arg493Trp
NM_001199400.2:c.1552A>T	NP_001186329.1:p.Arg518Trp
NM_001374418.1:c.1768A>T	NP_001361347.1:p.Arg590Trp
NM_001374419.1:c.1684A>T	NP_001361348.1:p.Arg562Trp
NM_001374420.1:c.1633A>T	NP_001361349.1:p.Arg545Trp
NM_001374421.1:c.1558A>T	NP_001361350.1:p.Arg520Trp
NM_012224.3:c.1684A>T	NP_036356.1:p.Arg562Trp
NR_164630.1:n.2230A>T
NM_001199398.3:c.1636A>T	NP_001186327.1:p.Arg546Trp
NM_001199399.3:c.1477A>T	NP_001186328.1:p.Arg493Trp
NM_001199400.3:c.1552A>T	NP_001186329.1:p.Arg518Trp
NM_012224.4:c.1684A>T	NP_036356.1:p.Arg562Trp