Canonical Allele Identifier: CA541728001

Gene: NEK10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.27297174C>G , CM000665.2:g.27297174C>G	GRCh38
NC_000003.11:g.27338665C>G , CM000665.1:g.27338665C>G	GRCh37
NC_000003.10:g.27313669C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001394966.1:c.1230+5G>C MANE Select	NP_001381895.1:n.1230+5G>C
ENST00000691995.1:c.1230+5G>C MANE Select	ENSP00000509472.1:n.1230+5G>C
NM_001394963.1:c.1230+5G>C	NP_001381892.1:n.1230+5G>C
NM_001394964.1:c.1143+5G>C	NP_001381893.1:n.1143+5G>C
NM_001394965.1:c.1230+5G>C	NP_001381894.1:n.1230+5G>C
NM_001394967.1:c.1143+5G>C	NP_001381896.1:n.1143+5G>C
NM_001394968.1:c.1235G>C	NP_001381897.1:p.Arg412Thr
NM_001394969.1:c.1143+5G>C	NP_001381898.1:n.1143+5G>C
NM_001394970.1:c.1230+5G>C	NP_001381899.1:n.1230+5G>C
NM_001394971.1:c.1230+5G>C	NP_001381900.1:n.1230+5G>C
NM_152534.4:c.1230+5G>C	NP_689747.3:n.1230+5G>C
NM_152534.5:c.1230+5G>C	NP_689747.3:n.1230+5G>C
NM_152534.6:c.1230+5G>C	NP_689747.3:n.1230+5G>C
NM_199347.3:c.1230+5G>C	NP_955379.2:n.1230+5G>C
NM_199347.4:c.1230+5G>C	NP_955379.2:n.1230+5G>C
ENST00000341435.9:c.1230+5G>C	ENSP00000343847.5:n.1230+5G>C
ENST00000429845.6:c.1230+5G>C	ENSP00000395849.2:n.1230+5G>C
XM_006712997.2:c.1230+5G>C	XP_006713060.1:n.1230+5G>C
XM_006712997.3:c.1230+5G>C	XP_006713060.1:n.1230+5G>C
XM_006712998.2:c.1230+5G>C	XP_006713061.1:n.1230+5G>C
XM_006712999.2:c.1230+5G>C	XP_006713062.1:n.1230+5G>C
XM_006712999.3:c.1230+5G>C	XP_006713062.1:n.1230+5G>C
XM_006713001.2:c.1230+5G>C	XP_006713064.1:n.1230+5G>C
XM_006713001.3:c.1230+5G>C	XP_006713064.1:n.1230+5G>C
XM_006713002.1:c.1230+5G>C	XP_006713065.1:n.1230+5G>C
XM_011533404.1:c.1230+5G>C	XP_011531706.1:n.1230+5G>C
XM_011533405.1:c.1230+5G>C	XP_011531707.1:n.1230+5G>C
XM_011533406.1:c.1230+5G>C	XP_011531708.1:n.1230+5G>C
XM_011533407.1:c.1230+5G>C	XP_011531709.1:n.1230+5G>C
XM_011533408.1:c.1230+5G>C	XP_011531710.1:n.1230+5G>C
XM_011533409.1:c.1230+5G>C	XP_011531711.1:n.1230+5G>C
XM_011533410.1:c.1230+5G>C	XP_011531712.1:n.1230+5G>C
XM_011533411.1:c.1230+5G>C	XP_011531713.1:n.1230+5G>C
XM_011533412.1:c.1230+5G>C	XP_011531714.1:n.1230+5G>C
XM_011533413.1:c.1230+5G>C	XP_011531715.1:n.1230+5G>C
XM_011533413.2:c.1230+5G>C	XP_011531715.1:n.1230+5G>C
XM_011533414.1:c.1230+5G>C	XP_011531716.1:n.1230+5G>C
XM_011533414.2:c.1230+5G>C	XP_011531716.1:n.1230+5G>C
XM_011533415.1:c.1230+5G>C	XP_011531717.1:n.1230+5G>C
XM_017005761.2:c.1230+5G>C	XP_016861250.1:n.1230+5G>C
XM_017005762.2:c.1230+5G>C	XP_016861251.1:n.1230+5G>C
XM_017005763.1:c.1230+5G>C	XP_016861252.1:n.1230+5G>C
XM_017005764.1:c.1230+5G>C	XP_016861253.1:n.1230+5G>C
XM_017005765.1:c.1230+5G>C	XP_016861254.1:n.1230+5G>C
XM_017005766.2:c.1230+5G>C	XP_016861255.1:n.1230+5G>C
XM_017005767.2:c.1143+5G>C	XP_016861256.1:n.1143+5G>C
XM_017005768.1:c.1230+5G>C	XP_016861257.1:n.1230+5G>C
XM_017005769.1:c.1230+5G>C	XP_016861258.1:n.1230+5G>C
XM_017005770.2:c.1230+5G>C	XP_016861259.1:n.1230+5G>C
XM_017005771.2:c.1230+5G>C	XP_016861260.1:n.1230+5G>C
XM_017005772.2:c.1143+5G>C	XP_016861261.1:n.1143+5G>C
XM_017005773.1:c.1230+5G>C	XP_016861262.1:n.1230+5G>C
XM_017005774.2:c.1230+5G>C	XP_016861263.1:n.1230+5G>C
XM_024453373.1:c.1143+5G>C	XP_024309141.1:n.1143+5G>C
XM_024453374.1:c.-1463G>C	XP_024309142.1:n.-1463G>C
XR_001740034.1:n.1504+5G>C
XR_940384.1:n.1504+5G>C