Canonical Allele Identifier: CA467070858

Gene: CDK5RAP2

Linked Data

• MyVariant Identifiers: chr9:g.123201751C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120439473C>T , CM000671.2:g.120439473C>T	GRCh38
NC_000009.11:g.123201751C>T , CM000671.1:g.123201751C>T	GRCh37
NC_000009.10:g.122241572C>T	NCBI36
NG_008999.1:g.145687G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360822.8:c.2958G>A	ENSP00000354065.4:p.Glu986=
ENST00000416449.6:c.3552G>A	ENSP00000400395.2:p.Glu1184=
ENST00000479584.2:n.1895G>A
ENST00000684780.1:n.3938G>A
ENST00000685866.1:c.*1475G>A	ENSP00000509484.1:n.*1475G>A
ENST00000686376.1:c.3728G>A	ENSP00000510021.1:n.3728G>A
ENST00000686842.1:n.7202G>A
ENST00000687279.1:c.3645G>A	ENSP00000508692.1:p.Glu1215=
ENST00000687311.1:n.3611G>A
ENST00000687633.1:c.3549G>A	ENSP00000510289.1:p.Glu1183=
ENST00000688923.1:n.3020G>A
ENST00000689688.1:c.3648G>A	ENSP00000510155.1:p.Glu1216=
ENST00000690646.1:c.3552G>A	ENSP00000510383.1:p.Glu1184=
ENST00000690814.1:c.*824G>A	ENSP00000508792.1:n.*824G>A
ENST00000691504.1:n.3542G>A
ENST00000692155.1:c.3728G>A	ENSP00000510290.1:n.3728G>A
ENST00000692746.1:n.3555G>A
ENST00000693386.1:c.3552G>A	ENSP00000510003.1:p.Glu1184=
ENST00000693433.1:n.3542G>A
ENST00000693714.1:n.3595G>A
ENST00000693728.1:c.3552G>A	ENSP00000510580.1:p.Glu1184=
ENST00000349780.9:c.3648G>A MANE Select	ENSP00000343818.4:p.Glu1216=
ENST00000349780.8:c.3648G>A	ENSP00000343818.4:p.Glu1216=
ENST00000360190.8:c.3648G>A	ENSP00000353317.4:p.Glu1216=
ENST00000360822.7:c.2958G>A	ENSP00000354065.4:p.Glu986=
ENST00000416449.5:c.1830G>A	ENSP00000400395.1:p.Glu610=
ENST00000425647.1:c.678G>A	ENSP00000409941.1:p.Glu226=
ENST00000473282.6:c.*2472G>A	ENSP00000419265.1:n.*2472G>A
ENST00000480112.5:c.*1475G>A	ENSP00000418418.1:n.*1475G>A
ENST00000483412.5:n.2956G>A
NM_001011649.2:c.3648G>A	NP_001011649.1:p.Glu1216=
NM_001272039.1:c.2958G>A	NP_001258968.1:p.Glu986=
NM_018249.5:c.3648G>A	NP_060719.4:p.Glu1216=
NR_073554.1:n.3917G>A
NR_073555.1:n.3840G>A
NR_073556.1:n.4047G>A
NR_073557.1:n.3920G>A
NR_073558.1:n.3917G>A
XM_006717182.1:c.3552G>A	XP_006717245.1:p.Glu1184=
XM_006717185.1:c.2961G>A	XP_006717248.1:p.Glu987=
XM_011518860.1:c.3645G>A	XP_011517162.1:p.Glu1215=
XM_011518861.1:c.3645G>A	XP_011517163.1:p.Glu1215=
XM_017014921.1:c.3549G>A	XP_016870410.1:p.Glu1183=
XM_017014922.1:c.2814G>A	XP_016870411.1:p.Glu938=
XM_017014923.1:c.2961G>A	XP_016870412.1:p.Glu987=
XM_017014924.1:c.1443G>A	XP_016870413.1:p.Glu481=
NM_018249.6:c.3648G>A MANE Select	NP_060719.4:p.Glu1216=
NM_001011649.3:c.3648G>A	NP_001011649.1:p.Glu1216=
NR_073554.2:n.3914G>A
NR_073555.2:n.3837G>A
NR_073556.2:n.4044G>A
NR_073557.2:n.3917G>A
NR_073558.2:n.3914G>A
NM_001272039.2:c.2958G>A	NP_001258968.1:p.Glu986=