Canonical Allele Identifier: CA266133257

Gene: CCNK

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.99492837G>A , CM000676.2:g.99492837G>A	GRCh38
NC_000014.8:g.99959174G>A , CM000676.1:g.99959174G>A	GRCh37
NC_000014.7:g.99028927G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001099402.2:c.160G>A MANE Select	NP_001092872.1:p.Ala54Thr
ENST00000389879.9:c.160G>A MANE Select	ENSP00000374529.5:p.Ala54Thr
NM_001099402.1:c.160G>A	NP_001092872.1:p.Ala54Thr
ENST00000553636.1:n.280G>A
ENST00000555049.5:c.160G>A	ENSP00000452307.1:p.Ala54Thr
ENST00000555842.1:c.160G>A	ENSP00000450440.1:p.Ala54Thr
ENST00000556641.5:n.242G>A
ENST00000557165.5:n.428G>A
ENST00000557441.5:c.160G>A	ENSP00000450792.1:p.Ala54Thr
XM_005268154.3:c.160G>A	XP_005268211.1:p.Ala54Thr
XM_005268154.4:c.160G>A	XP_005268211.1:p.Ala54Thr
XM_011537275.1:c.160G>A	XP_011535577.1:p.Ala54Thr
XM_011537275.2:c.160G>A	XP_011535577.1:p.Ala54Thr