Canonical Allele Identifier: CA10584042

Gene: NEK9 ZC2HC1C

Linked Data

• dbSNP Id: rs886037839
• MyVariant Identifiers: chr14:g.75570561C>A (hg19) ; chr14:g.75103858C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75103858C>A , CM000676.2:g.75103858C>A	GRCh38
NC_000014.8:g.75570561C>A , CM000676.1:g.75570561C>A	GRCh37
NC_000014.7:g.74640314C>A	NCBI36
NG_051093.1:g.28223G>T

Transcript Alleles

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