Canonical Allele Identifier: CA1876636232
Gene: CDK5RAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120439486T= , CM000671.2:g.120439486T= GRCh38
NC_000009.11:g.123201764T= , CM000671.1:g.123201764T= GRCh37
NC_000009.10:g.122241585T= NCBI36
NG_008999.1:g.145674A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360822.8:c.2945A= ENSP00000354065.4:p.Lys982=
ENST00000416449.6:c.3539A= ENSP00000400395.2:p.Lys1180=
ENST00000479584.2:n.1882A=
ENST00000684780.1:n.3925A=
ENST00000685866.1:c.*1462A= ENSP00000509484.1:n.*1462A=
ENST00000686376.1:c.3715A= ENSP00000510021.1:n.3715A=
ENST00000686842.1:n.7189A=
ENST00000687279.1:c.3632A= ENSP00000508692.1:p.Lys1211=
ENST00000687311.1:n.3598A=
ENST00000687633.1:c.3536A= ENSP00000510289.1:p.Lys1179=
ENST00000688923.1:n.3007A=
ENST00000689688.1:c.3635A= ENSP00000510155.1:p.Lys1212=
ENST00000690646.1:c.3539A= ENSP00000510383.1:p.Lys1180=
ENST00000690814.1:c.*811A= ENSP00000508792.1:n.*811A=
ENST00000691504.1:n.3529A=
ENST00000692155.1:c.3715A= ENSP00000510290.1:n.3715A=
ENST00000692746.1:n.3542A=
ENST00000693386.1:c.3539A= ENSP00000510003.1:p.Lys1180=
ENST00000693433.1:n.3529A=
ENST00000693714.1:n.3582A=
ENST00000693728.1:c.3539A= ENSP00000510580.1:p.Lys1180=
ENST00000349780.9:c.3635A= MANE Select ENSP00000343818.4:p.Lys1212=
ENST00000349780.8:c.3635A= ENSP00000343818.4:p.Lys1212=
ENST00000360190.8:c.3635A= ENSP00000353317.4:p.Lys1212=
ENST00000360822.7:c.2945A= ENSP00000354065.4:p.Lys982=
ENST00000416449.5:c.1817A= ENSP00000400395.1:p.Lys606=
ENST00000425647.1:c.665A= ENSP00000409941.1:p.Lys222=
ENST00000473282.6:c.*2459A= ENSP00000419265.1:n.*2459A=
ENST00000480112.5:c.*1462A= ENSP00000418418.1:n.*1462A=
ENST00000483412.5:n.2943A=
NM_001011649.2:c.3635A= NP_001011649.1:p.Lys1212=
NM_001272039.1:c.2945A= NP_001258968.1:p.Lys982=
NM_018249.5:c.3635A= NP_060719.4:p.Lys1212=
NR_073554.1:n.3904A=
NR_073555.1:n.3827A=
NR_073556.1:n.4034A=
NR_073557.1:n.3907A=
NR_073558.1:n.3904A=
XM_006717182.1:c.3539A= XP_006717245.1:p.Lys1180=
XM_006717185.1:c.2948A= XP_006717248.1:p.Lys983=
XM_011518860.1:c.3632A= XP_011517162.1:p.Lys1211=
XM_011518861.1:c.3632A= XP_011517163.1:p.Lys1211=
XM_017014921.1:c.3536A= XP_016870410.1:p.Lys1179=
XM_017014922.1:c.2801A= XP_016870411.1:p.Lys934=
XM_017014923.1:c.2948A= XP_016870412.1:p.Lys983=
XM_017014924.1:c.1430A= XP_016870413.1:p.Lys477=
NM_018249.6:c.3635A= MANE Select NP_060719.4:p.Lys1212=
NM_001011649.3:c.3635A= NP_001011649.1:p.Lys1212=
NR_073554.2:n.3901A=
NR_073555.2:n.3824A=
NR_073556.2:n.4031A=
NR_073557.2:n.3904A=
NR_073558.2:n.3901A=
NM_001272039.2:c.2945A= NP_001258968.1:p.Lys982=