Canonical Allele Identifier: CA2838508115

Gene: NEK6

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124339680G>T , CM000671.2:g.124339680G>T	GRCh38
NC_000009.11:g.127101959G>T , CM000671.1:g.127101959G>T	GRCh37
NC_000009.10:g.126141780G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320246.10:c.717+15G>T MANE Select	ENSP00000319734.5:n.717+15G>T
ENST00000320246.9:c.717+15G>T	ENSP00000319734.5:n.717+15G>T
ENST00000373600.7:c.819+15G>T	ENSP00000362702.3:n.819+15G>T
ENST00000373603.5:c.717+15G>T	ENSP00000362705.1:n.717+15G>T
ENST00000394199.6:c.819+15G>T	ENSP00000377749.2:n.819+15G>T
ENST00000454453.5:c.513+15G>T	ENSP00000405215.1:n.513+15G>T
ENST00000539416.5:c.792+15G>T	ENSP00000439651.1:n.792+15G>T
ENST00000540326.5:c.771+15G>T	ENSP00000441469.1:n.771+15G>T
ENST00000545174.5:c.717+15G>T	ENSP00000442636.1:n.717+15G>T
ENST00000546191.5:c.717+15G>T	ENSP00000441426.1:n.717+15G>T
NM_001145001.2:c.819+15G>T	NP_001138473.1:n.819+15G>T
NM_001166167.1:c.771+15G>T	NP_001159639.1:n.771+15G>T
NM_001166168.1:c.717+15G>T	NP_001159640.1:n.717+15G>T
NM_001166169.1:c.792+15G>T	NP_001159641.1:n.792+15G>T
NM_001166170.1:c.717+15G>T	NP_001159642.1:n.717+15G>T
NM_001166171.1:c.819+15G>T	NP_001159643.1:n.819+15G>T
NM_014397.5:c.717+15G>T	NP_055212.2:n.717+15G>T
XM_005251664.1:c.717+15G>T	XP_005251721.1:n.717+15G>T
XM_006716936.1:c.717+15G>T	XP_006716999.1:n.717+15G>T
XM_011518155.1:c.717+15G>T	XP_011516457.1:n.717+15G>T
XM_006716936.2:c.717+15G>T	XP_006716999.1:n.717+15G>T
XM_017014217.1:c.819+15G>T	XP_016869706.1:n.819+15G>T
XM_024447385.1:c.891+15G>T	XP_024303153.1:n.891+15G>T
XM_024447386.1:c.717+15G>T	XP_024303154.1:n.717+15G>T
XM_024447387.1:c.717+15G>T	XP_024303155.1:n.717+15G>T
NM_001145001.3:c.819+15G>T	NP_001138473.1:n.819+15G>T
NM_001166167.2:c.771+15G>T	NP_001159639.1:n.771+15G>T
NM_001166168.2:c.717+15G>T	NP_001159640.1:n.717+15G>T
NM_001166169.2:c.792+15G>T	NP_001159641.1:n.792+15G>T
NM_001166170.2:c.717+15G>T	NP_001159642.1:n.717+15G>T
NM_001166171.2:c.819+15G>T	NP_001159643.1:n.819+15G>T
NM_014397.6:c.717+15G>T MANE Select	NP_055212.2:n.717+15G>T