Canonical Allele Identifier: CA442293282

Gene: NEK1

Linked Data

• gnomAD v4: 4-169508805-A-G
• MyVariant Identifiers: chr4:g.170429956A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.169508805A>G , CM000666.2:g.169508805A>G	GRCh38
NC_000004.11:g.170429956A>G , CM000666.1:g.170429956A>G	GRCh37
NC_000004.10:g.170666531A>G	NCBI36
NG_027982.1:g.108823T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685111.1:c.1582-474T>C	ENSP00000508844.1:n.1582-474T>C
ENST00000685677.1:n.1011T>C
ENST00000686697.1:c.1540-474T>C	ENSP00000508689.1:n.1540-474T>C
ENST00000687054.1:n.2244-474T>C
ENST00000687219.1:c.*1253-474T>C	ENSP00000509736.1:n.*1253-474T>C
ENST00000687528.1:c.1581T>C	ENSP00000510228.1:p.Ser527=
ENST00000687643.1:c.1693-474T>C	ENSP00000509309.1:n.1693-474T>C
ENST00000688934.1:c.-132-474T>C	ENSP00000510760.1:n.-132-474T>C
ENST00000689190.1:n.1162T>C
ENST00000692450.1:c.*1378T>C	ENSP00000510283.1:n.*1378T>C
ENST00000693085.1:c.*1493-474T>C	ENSP00000508746.1:n.*1493-474T>C
ENST00000693604.1:c.*684-474T>C	ENSP00000509917.1:n.*684-474T>C
ENST00000507142.6:c.1713T>C MANE Select	ENSP00000424757.2:p.Ser571=
ENST00000439128.6:c.1666-474T>C	ENSP00000408020.2:n.1666-474T>C
ENST00000507142.5:c.1713T>C	ENSP00000424757.1:p.Ser571=
ENST00000510533.5:c.1534-474T>C	ENSP00000427653.1:n.1534-474T>C
ENST00000511633.5:c.1581T>C	ENSP00000423332.1:p.Ser527=
ENST00000512193.5:c.1459-474T>C	ENSP00000424938.1:n.1459-474T>C
NM_001199397.1:c.1713T>C	NP_001186326.1:p.Ser571=
NM_001199398.1:c.1581T>C	NP_001186327.1:p.Ser527=
NM_001199399.1:c.1459-474T>C	NP_001186328.1:n.1459-474T>C
NM_001199400.1:c.1534-474T>C	NP_001186329.1:n.1534-474T>C
NM_012224.2:c.1666-474T>C	NP_036356.1:n.1666-474T>C
XM_006714228.1:c.1713T>C	XP_006714291.1:p.Ser571=
XM_011532003.1:c.1666-474T>C	XP_011530305.1:n.1666-474T>C
XM_011532004.1:c.1534-474T>C	XP_011530306.1:n.1534-474T>C
XM_011532005.1:c.1713T>C	XP_011530307.1:p.Ser571=
XM_011532005.2:c.1713T>C	XP_011530307.1:p.Ser571=
XM_017008249.1:c.1092T>C	XP_016863738.1:p.Ser364=
XM_017008251.1:c.1045-474T>C	XP_016863740.1:n.1045-474T>C
XM_017008252.2:c.1045-474T>C	XP_016863741.1:n.1045-474T>C
XM_017008253.1:c.561T>C	XP_016863742.1:p.Ser187=
XM_017008254.1:c.357T>C	XP_016863743.1:p.Ser119=
XM_024454065.1:c.1092T>C	XP_024309833.1:p.Ser364=
XR_001741233.1:n.2293T>C
XR_001741234.2:n.2106T>C
NM_001199397.3:c.1713T>C MANE Select	NP_001186326.1:p.Ser571=
NM_001199398.2:c.1581T>C	NP_001186327.1:p.Ser527=
NM_001199399.2:c.1459-474T>C	NP_001186328.1:n.1459-474T>C
NM_001199400.2:c.1534-474T>C	NP_001186329.1:n.1534-474T>C
NM_001374418.1:c.1713T>C	NP_001361347.1:p.Ser571=
NM_001374419.1:c.1666-474T>C	NP_001361348.1:n.1666-474T>C
NM_001374420.1:c.1615-474T>C	NP_001361349.1:n.1615-474T>C
NM_001374421.1:c.1540-474T>C	NP_001361350.1:n.1540-474T>C
NM_012224.3:c.1666-474T>C	NP_036356.1:n.1666-474T>C
NR_164630.1:n.2212-474T>C
NM_001199398.3:c.1581T>C	NP_001186327.1:p.Ser527=
NM_001199399.3:c.1459-474T>C	NP_001186328.1:n.1459-474T>C
NM_001199400.3:c.1534-474T>C	NP_001186329.1:n.1534-474T>C
NM_012224.4:c.1666-474T>C	NP_036356.1:n.1666-474T>C