Canonical Allele Identifier: CA358800846
Community Standard Title: NM_001199397.3(NEK1):c.3337G>T (p.Glu1113Ter)
Gene: NEK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.169406633C>A , CM000666.2:g.169406633C>A GRCh38
NC_000004.11:g.170327784C>A , CM000666.1:g.170327784C>A GRCh37
NC_000004.10:g.170564359C>A NCBI36
NG_027982.1:g.210995G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001199397.3:c.3337G>T MANE Select NP_001186326.1:p.Glu1113Ter
ENST00000507142.6:c.3337G>T MANE Select ENSP00000424757.2:p.Glu1113Ter
NM_001199397.1:c.3337G>T NP_001186326.1:p.Glu1113Ter
NM_001199398.1:c.3205G>T NP_001186327.1:p.Glu1069Ter
NM_001199398.2:c.3205G>T NP_001186327.1:p.Glu1069Ter
NM_001199398.3:c.3205G>T NP_001186327.1:p.Glu1069Ter
NM_001199399.1:c.3046G>T NP_001186328.1:p.Glu1016Ter
NM_001199399.2:c.3046G>T NP_001186328.1:p.Glu1016Ter
NM_001199399.3:c.3046G>T NP_001186328.1:p.Glu1016Ter
NM_001199400.1:c.3121G>T NP_001186329.1:p.Glu1041Ter
NM_001199400.2:c.3121G>T NP_001186329.1:p.Glu1041Ter
NM_001199400.3:c.3121G>T NP_001186329.1:p.Glu1041Ter
NM_001374418.1:c.3337G>T NP_001361347.1:p.Glu1113Ter
NM_001374419.1:c.3253G>T NP_001361348.1:p.Glu1085Ter
NM_001374420.1:c.3202G>T NP_001361349.1:p.Glu1068Ter
NM_001374421.1:c.2854G>T NP_001361350.1:p.Glu952Ter
NM_012224.2:c.3253G>T NP_036356.1:p.Glu1085Ter
NM_012224.3:c.3253G>T NP_036356.1:p.Glu1085Ter
NM_012224.4:c.3253G>T NP_036356.1:p.Glu1085Ter
NR_164630.1:n.3799G>T
ENST00000439128.6:c.3253G>T ENSP00000408020.2:p.Glu1085Ter
ENST00000507142.5:c.3337G>T ENSP00000424757.1:p.Glu1113Ter
ENST00000510533.5:c.3121G>T ENSP00000427653.1:p.Glu1041Ter
ENST00000511633.5:c.3205G>T ENSP00000423332.1:p.Glu1069Ter
ENST00000512193.5:c.3046G>T ENSP00000424938.1:p.Glu1016Ter
ENST00000638824.1:n.1465G>T
ENST00000685111.1:c.3169G>T ENSP00000508844.1:p.Glu1057Ter
ENST00000685677.1:n.2635G>T
ENST00000686697.1:c.2854G>T ENSP00000508689.1:p.Glu952Ter
ENST00000687054.1:n.3831G>T
ENST00000687528.1:c.*2072G>T ENSP00000510228.1:n.*2072G>T
ENST00000687643.1:c.3280G>T ENSP00000509309.1:p.Glu1094Ter
ENST00000688934.1:c.1360G>T ENSP00000510760.1:p.Glu454Ter
ENST00000690540.1:n.2787G>T
XM_006714228.1:c.3160G>T XP_006714291.1:p.Glu1054Ter
XM_011532003.1:c.3253G>T XP_011530305.1:p.Glu1085Ter
XM_011532004.1:c.3121G>T XP_011530306.1:p.Glu1041Ter
XM_017008249.1:c.2716G>T XP_016863738.1:p.Glu906Ter
XM_017008251.1:c.2632G>T XP_016863740.1:p.Glu878Ter
XM_017008252.2:c.2632G>T XP_016863741.1:p.Glu878Ter
XM_017008253.1:c.2185G>T XP_016863742.1:p.Glu729Ter
XM_017008254.1:c.1981G>T XP_016863743.1:p.Glu661Ter
XM_024454065.1:c.2716G>T XP_024309833.1:p.Glu906Ter
XR_001741233.1:n.3622G>T