Canonical Allele Identifier: CA3137764

Gene: NEK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.169556027A>G , CM000666.2:g.169556027A>G	GRCh38
NC_000004.11:g.170477178A>G , CM000666.1:g.170477178A>G	GRCh37
NC_000004.10:g.170713753A>G	NCBI36
NG_027982.1:g.61601T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001199397.3:c.1335T>C MANE Select	NP_001186326.1:p.His445=
ENST00000507142.6:c.1335T>C MANE Select	ENSP00000424757.2:p.His445=
NM_001199397.1:c.1335T>C	NP_001186326.1:p.His445=
NM_001199398.1:c.1335T>C	NP_001186327.1:p.His445=
NM_001199398.2:c.1335T>C	NP_001186327.1:p.His445=
NM_001199398.3:c.1335T>C	NP_001186327.1:p.His445=
NM_001199399.1:c.1260T>C	NP_001186328.1:p.His420=
NM_001199399.2:c.1260T>C	NP_001186328.1:p.His420=
NM_001199399.3:c.1260T>C	NP_001186328.1:p.His420=
NM_001199400.1:c.1335T>C	NP_001186329.1:p.His445=
NM_001199400.2:c.1335T>C	NP_001186329.1:p.His445=
NM_001199400.3:c.1335T>C	NP_001186329.1:p.His445=
NM_001374418.1:c.1335T>C	NP_001361347.1:p.His445=
NM_001374419.1:c.1335T>C	NP_001361348.1:p.His445=
NM_001374420.1:c.1284T>C	NP_001361349.1:p.His428=
NM_001374421.1:c.1209T>C	NP_001361350.1:p.His403=
NM_012224.2:c.1335T>C	NP_036356.1:p.His445=
NM_012224.3:c.1335T>C	NP_036356.1:p.His445=
NM_012224.4:c.1335T>C	NP_036356.1:p.His445=
NR_164630.1:n.1849T>C
ENST00000439128.6:c.1335T>C	ENSP00000408020.2:p.His445=
ENST00000507142.5:c.1335T>C	ENSP00000424757.1:p.His445=
ENST00000509912.5:n.1067T>C
ENST00000510533.5:c.1335T>C	ENSP00000427653.1:p.His445=
ENST00000511633.5:c.1335T>C	ENSP00000423332.1:p.His445=
ENST00000512193.5:c.1260T>C	ENSP00000424938.1:p.His420=
ENST00000685111.1:c.1251T>C	ENSP00000508844.1:p.His417=
ENST00000685677.1:n.633T>C
ENST00000686697.1:c.1209T>C	ENSP00000508689.1:p.His403=
ENST00000687054.1:n.1913T>C
ENST00000687219.1:c.*922T>C	ENSP00000509736.1:n.*922T>C
ENST00000687528.1:c.1335T>C	ENSP00000510228.1:p.His445=
ENST00000687643.1:c.1362T>C	ENSP00000509309.1:p.His454=
ENST00000688487.1:n.1698T>C
ENST00000688934.1:c.-132-47696T>C	ENSP00000510760.1:n.-132-47696T>C
ENST00000690631.1:n.1912T>C
ENST00000692450.1:c.*1132T>C	ENSP00000510283.1:n.*1132T>C
ENST00000693085.1:c.*1162T>C	ENSP00000508746.1:n.*1162T>C
ENST00000693604.1:c.*353T>C	ENSP00000509917.1:n.*353T>C
XM_006714228.1:c.1335T>C	XP_006714291.1:p.His445=
XM_011532003.1:c.1335T>C	XP_011530305.1:p.His445=
XM_011532004.1:c.1335T>C	XP_011530306.1:p.His445=
XM_011532005.1:c.1335T>C	XP_011530307.1:p.His445=
XM_011532005.2:c.1335T>C	XP_011530307.1:p.His445=
XM_017008249.1:c.714T>C	XP_016863738.1:p.His238=
XM_017008251.1:c.714T>C	XP_016863740.1:p.His238=
XM_017008252.2:c.714T>C	XP_016863741.1:p.His238=
XM_017008253.1:c.183T>C	XP_016863742.1:p.His61=
XM_017008254.1:c.-22T>C	XP_016863743.1:n.-22T>C
XM_024454065.1:c.714T>C	XP_024309833.1:p.His238=
XR_001741233.1:n.1915T>C
XR_001741234.2:n.1860T>C