Canonical Allele Identifier: CA358731779

Gene: NEK1

Linked Data

• MyVariant Identifiers: chr4:g.170429463C>G (hg19) ; chr4:g.169508312C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.169508312C>G , CM000666.2:g.169508312C>G	GRCh38
NC_000004.11:g.170429463C>G , CM000666.1:g.170429463C>G	GRCh37
NC_000004.10:g.170666038C>G	NCBI36
NG_027982.1:g.109316G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685111.1:c.1601G>C	ENSP00000508844.1:p.Arg534Thr
ENST00000685677.1:n.1067G>C
ENST00000686697.1:c.1559G>C	ENSP00000508689.1:p.Arg520Thr
ENST00000687054.1:n.2263G>C
ENST00000687219.1:c.*1272G>C	ENSP00000509736.1:n.*1272G>C
ENST00000687528.1:c.1637G>C	ENSP00000510228.1:p.Arg546Thr
ENST00000687643.1:c.1712G>C	ENSP00000509309.1:p.Arg571Thr
ENST00000688934.1:c.-113G>C	ENSP00000510760.1:n.-113G>C
ENST00000689190.1:n.1655G>C
ENST00000692450.1:c.*1434G>C	ENSP00000510283.1:n.*1434G>C
ENST00000693085.1:c.*1512G>C	ENSP00000508746.1:n.*1512G>C
ENST00000693604.1:c.*703G>C	ENSP00000509917.1:n.*703G>C
ENST00000507142.6:c.1769G>C MANE Select	ENSP00000424757.2:p.Arg590Thr
ENST00000439128.6:c.1685G>C	ENSP00000408020.2:p.Arg562Thr
ENST00000507142.5:c.1769G>C	ENSP00000424757.1:p.Arg590Thr
ENST00000510533.5:c.1553G>C	ENSP00000427653.1:p.Arg518Thr
ENST00000511633.5:c.1637G>C	ENSP00000423332.1:p.Arg546Thr
ENST00000512193.5:c.1478G>C	ENSP00000424938.1:p.Arg493Thr
NM_001199397.1:c.1769G>C	NP_001186326.1:p.Arg590Thr
NM_001199398.1:c.1637G>C	NP_001186327.1:p.Arg546Thr
NM_001199399.1:c.1478G>C	NP_001186328.1:p.Arg493Thr
NM_001199400.1:c.1553G>C	NP_001186329.1:p.Arg518Thr
NM_012224.2:c.1685G>C	NP_036356.1:p.Arg562Thr
XM_006714228.1:c.1769G>C	XP_006714291.1:p.Arg590Thr
XM_011532003.1:c.1685G>C	XP_011530305.1:p.Arg562Thr
XM_011532004.1:c.1553G>C	XP_011530306.1:p.Arg518Thr
XM_011532005.1:c.1769G>C	XP_011530307.1:p.Arg590Thr
XM_011532005.2:c.1769G>C	XP_011530307.1:p.Arg590Thr
XM_017008249.1:c.1148G>C	XP_016863738.1:p.Arg383Thr
XM_017008251.1:c.1064G>C	XP_016863740.1:p.Arg355Thr
XM_017008252.2:c.1064G>C	XP_016863741.1:p.Arg355Thr
XM_017008253.1:c.617G>C	XP_016863742.1:p.Arg206Thr
XM_017008254.1:c.413G>C	XP_016863743.1:p.Arg138Thr
XM_024454065.1:c.1148G>C	XP_024309833.1:p.Arg383Thr
XR_001741233.1:n.2349G>C
XR_001741234.2:n.2162G>C
NM_001199397.3:c.1769G>C MANE Select	NP_001186326.1:p.Arg590Thr
NM_001199398.2:c.1637G>C	NP_001186327.1:p.Arg546Thr
NM_001199399.2:c.1478G>C	NP_001186328.1:p.Arg493Thr
NM_001199400.2:c.1553G>C	NP_001186329.1:p.Arg518Thr
NM_001374418.1:c.1769G>C	NP_001361347.1:p.Arg590Thr
NM_001374419.1:c.1685G>C	NP_001361348.1:p.Arg562Thr
NM_001374420.1:c.1634G>C	NP_001361349.1:p.Arg545Thr
NM_001374421.1:c.1559G>C	NP_001361350.1:p.Arg520Thr
NM_012224.3:c.1685G>C	NP_036356.1:p.Arg562Thr
NR_164630.1:n.2231G>C
NM_001199398.3:c.1637G>C	NP_001186327.1:p.Arg546Thr
NM_001199399.3:c.1478G>C	NP_001186328.1:p.Arg493Thr
NM_001199400.3:c.1553G>C	NP_001186329.1:p.Arg518Thr
NM_012224.4:c.1685G>C	NP_036356.1:p.Arg562Thr