Canonical Allele Identifier: CA645372566

Gene: NEK9 ZC2HC1C

Linked Data

• PubMed: PMID:27153399

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.[75103841C>A;75103858C>A] , CM000676.2:g.[75103841C>A;75103858C>A]	GRCh38
NC_000014.8:g.[75570544C>A;75570561C>A] , CM000676.1:g.[75570544C>A;75570561C>A]	GRCh37
NC_000014.7:g.[74640297C>A;74640314C>A]	NCBI36
NG_051093.1:g.[28223G>T;28240G>T]

Transcript Alleles

HGVS	Amino-acid Change
ENST00000238616.10:c.[1715G>T;1731+1G>T] (NEK9) MANE Select	ENSP00000238616.5:p.Gly572Val
ENST00000553823.6:c.[1715G>T;1732G>T] (NEK9)	ENSP00000452537.2:p.[Gly572Val;Val578Leu]
ENST00000673981.1:c.[*80-5046C>A;*80-5029C>A] (ZC2HC1C)	ENSP00000501014.1:n.[*80-5046C>A;*80-5029C>A]
ENST00000676476.1:n.[282G>T;298+1G>T] (NEK9)
ENST00000676711.1:n.[453G>T;469+1G>T] (NEK9)
ENST00000677700.1:c.[1617G>T;1633+1G>T] (NEK9)
ENST00000678037.1:c.[1751G>T;1767+1G>T] (NEK9)	ENSP00000504620.1:p.Gly584Val
ENST00000678531.1:c.[1361G>T;1377+1G>T] (NEK9)	ENSP00000503827.1:p.Gly454Val
ENST00000678749.1:c.[1361G>T;1377+1G>T] (NEK9)	ENSP00000504104.1:p.Gly454Val
ENST00000238616.9:c.[1715G>T;1731+1G>T] (NEK9)	ENSP00000238616.5:p.Gly572Val
ENST00000556170.5:n.[2344G>T;2360+1G>T] (NEK9)
ENST00000557026.5:n.[1509G>T;1525+1G>T] (NEK9)
NM_033116.4:c.[1715G>T;1731+1G>T] (NEK9)	NP_149107.4:p.Gly572Val
XM_005268208.1:c.[1751G>T;1767+1G>T] (NEK9)	XP_005268265.1:p.Gly584Val
XM_005268209.2:c.[1397G>T;1413+1G>T] (NEK9)	XP_005268266.1:p.Gly466Val
NM_001329237.1:c.[1751G>T;1767+1G>T] (NEK9)	NP_001316166.1:p.Gly584Val
NM_001329238.1:c.[1361G>T;1377+1G>T] (NEK9)	NP_001316167.1:p.Gly454Val
NM_033116.5:c.[1715G>T;1731+1G>T] (NEK9)	NP_149107.4:p.Gly572Val
XM_005268209.3:c.[1397G>T;1413+1G>T] (NEK9)	XP_005268266.1:p.Gly466Val
XM_024449741.1:c.[1397G>T;1413+1G>T] (NEK9)	XP_024305509.1:p.Gly466Val
NM_033116.6:c.[1715G>T;1731+1G>T] (NEK9) MANE Select	NP_149107.4:p.Gly572Val
NM_001329237.2:c.[1751G>T;1767+1G>T] (NEK9)	NP_001316166.1:p.Gly584Val
NM_001329238.2:c.[1361G>T;1377+1G>T] (NEK9)	NP_001316167.1:p.Gly454Val