Canonical Allele Identifier: CA442293296

Gene: NEK1

Linked Data

• gnomAD v4: 4-169508817-G-A
• MyVariant Identifiers: chr4:g.170429968G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.169508817G>A , CM000666.2:g.169508817G>A	GRCh38
NC_000004.11:g.170429968G>A , CM000666.1:g.170429968G>A	GRCh37
NC_000004.10:g.170666543G>A	NCBI36
NG_027982.1:g.108811C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685111.1:c.1582-486C>T	ENSP00000508844.1:n.1582-486C>T
ENST00000685677.1:n.999C>T
ENST00000686697.1:c.1540-486C>T	ENSP00000508689.1:n.1540-486C>T
ENST00000687054.1:n.2244-486C>T
ENST00000687219.1:c.*1253-486C>T	ENSP00000509736.1:n.*1253-486C>T
ENST00000687528.1:c.1569C>T	ENSP00000510228.1:p.Gly523=
ENST00000687643.1:c.1693-486C>T	ENSP00000509309.1:n.1693-486C>T
ENST00000688934.1:c.-132-486C>T	ENSP00000510760.1:n.-132-486C>T
ENST00000689190.1:n.1150C>T
ENST00000692450.1:c.*1366C>T	ENSP00000510283.1:n.*1366C>T
ENST00000693085.1:c.*1493-486C>T	ENSP00000508746.1:n.*1493-486C>T
ENST00000693604.1:c.*684-486C>T	ENSP00000509917.1:n.*684-486C>T
ENST00000507142.6:c.1701C>T MANE Select	ENSP00000424757.2:p.Gly567=
ENST00000439128.6:c.1666-486C>T	ENSP00000408020.2:n.1666-486C>T
ENST00000507142.5:c.1701C>T	ENSP00000424757.1:p.Gly567=
ENST00000510533.5:c.1534-486C>T	ENSP00000427653.1:n.1534-486C>T
ENST00000511633.5:c.1569C>T	ENSP00000423332.1:p.Gly523=
ENST00000512193.5:c.1459-486C>T	ENSP00000424938.1:n.1459-486C>T
NM_001199397.1:c.1701C>T	NP_001186326.1:p.Gly567=
NM_001199398.1:c.1569C>T	NP_001186327.1:p.Gly523=
NM_001199399.1:c.1459-486C>T	NP_001186328.1:n.1459-486C>T
NM_001199400.1:c.1534-486C>T	NP_001186329.1:n.1534-486C>T
NM_012224.2:c.1666-486C>T	NP_036356.1:n.1666-486C>T
XM_006714228.1:c.1701C>T	XP_006714291.1:p.Gly567=
XM_011532003.1:c.1666-486C>T	XP_011530305.1:n.1666-486C>T
XM_011532004.1:c.1534-486C>T	XP_011530306.1:n.1534-486C>T
XM_011532005.1:c.1701C>T	XP_011530307.1:p.Gly567=
XM_011532005.2:c.1701C>T	XP_011530307.1:p.Gly567=
XM_017008249.1:c.1080C>T	XP_016863738.1:p.Gly360=
XM_017008251.1:c.1045-486C>T	XP_016863740.1:n.1045-486C>T
XM_017008252.2:c.1045-486C>T	XP_016863741.1:n.1045-486C>T
XM_017008253.1:c.549C>T	XP_016863742.1:p.Gly183=
XM_017008254.1:c.345C>T	XP_016863743.1:p.Gly115=
XM_024454065.1:c.1080C>T	XP_024309833.1:p.Gly360=
XR_001741233.1:n.2281C>T
XR_001741234.2:n.2094C>T
NM_001199397.3:c.1701C>T MANE Select	NP_001186326.1:p.Gly567=
NM_001199398.2:c.1569C>T	NP_001186327.1:p.Gly523=
NM_001199399.2:c.1459-486C>T	NP_001186328.1:n.1459-486C>T
NM_001199400.2:c.1534-486C>T	NP_001186329.1:n.1534-486C>T
NM_001374418.1:c.1701C>T	NP_001361347.1:p.Gly567=
NM_001374419.1:c.1666-486C>T	NP_001361348.1:n.1666-486C>T
NM_001374420.1:c.1615-486C>T	NP_001361349.1:n.1615-486C>T
NM_001374421.1:c.1540-486C>T	NP_001361350.1:n.1540-486C>T
NM_012224.3:c.1666-486C>T	NP_036356.1:n.1666-486C>T
NR_164630.1:n.2212-486C>T
NM_001199398.3:c.1569C>T	NP_001186327.1:p.Gly523=
NM_001199399.3:c.1459-486C>T	NP_001186328.1:n.1459-486C>T
NM_001199400.3:c.1534-486C>T	NP_001186329.1:n.1534-486C>T
NM_012224.4:c.1666-486C>T	NP_036356.1:n.1666-486C>T