Canonical Allele Identifier: CA1876636195
Gene: CDK5RAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120439400T= , CM000671.2:g.120439400T= GRCh38
NC_000009.11:g.123201678T= , CM000671.1:g.123201678T= GRCh37
NC_000009.10:g.122241499T= NCBI36
NG_008999.1:g.145760A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360822.8:c.3031A= ENSP00000354065.4:p.Arg1011=
ENST00000416449.6:c.3625A= ENSP00000400395.2:p.Arg1209=
ENST00000479584.2:n.1968A=
ENST00000684780.1:n.4011A=
ENST00000685866.1:c.*1548A= ENSP00000509484.1:n.*1548A=
ENST00000686376.1:c.3801A= ENSP00000510021.1:n.3801A=
ENST00000686842.1:n.7275A=
ENST00000687279.1:c.3718A= ENSP00000508692.1:p.Arg1240=
ENST00000687311.1:n.3684A=
ENST00000687633.1:c.3622A= ENSP00000510289.1:p.Arg1208=
ENST00000688923.1:n.3093A=
ENST00000689688.1:c.3721A= ENSP00000510155.1:p.Arg1241=
ENST00000690646.1:c.3625A= ENSP00000510383.1:p.Arg1209=
ENST00000690814.1:c.*897A= ENSP00000508792.1:n.*897A=
ENST00000691504.1:n.3615A=
ENST00000692155.1:c.3801A= ENSP00000510290.1:n.3801A=
ENST00000692746.1:n.3628A=
ENST00000693386.1:c.3625A= ENSP00000510003.1:p.Arg1209=
ENST00000693433.1:n.3615A=
ENST00000693714.1:n.3668A=
ENST00000693728.1:c.3625A= ENSP00000510580.1:p.Arg1209=
ENST00000349780.9:c.3721A= MANE Select ENSP00000343818.4:p.Arg1241=
ENST00000349780.8:c.3721A= ENSP00000343818.4:p.Arg1241=
ENST00000360190.8:c.3721A= ENSP00000353317.4:p.Arg1241=
ENST00000360822.7:c.3031A= ENSP00000354065.4:p.Arg1011=
ENST00000416449.5:c.1903A= ENSP00000400395.1:p.Arg635=
ENST00000425647.1:c.751A= ENSP00000409941.1:p.Arg251=
ENST00000473282.6:c.*2545A= ENSP00000419265.1:n.*2545A=
ENST00000480112.5:c.*1548A= ENSP00000418418.1:n.*1548A=
ENST00000483412.5:n.3029A=
NM_001011649.2:c.3721A= NP_001011649.1:p.Arg1241=
NM_001272039.1:c.3031A= NP_001258968.1:p.Arg1011=
NM_018249.5:c.3721A= NP_060719.4:p.Arg1241=
NR_073554.1:n.3990A=
NR_073555.1:n.3913A=
NR_073556.1:n.4120A=
NR_073557.1:n.3993A=
NR_073558.1:n.3990A=
XM_006717182.1:c.3625A= XP_006717245.1:p.Arg1209=
XM_006717185.1:c.3034A= XP_006717248.1:p.Arg1012=
XM_011518860.1:c.3718A= XP_011517162.1:p.Arg1240=
XM_011518861.1:c.3718A= XP_011517163.1:p.Arg1240=
XM_017014921.1:c.3622A= XP_016870410.1:p.Arg1208=
XM_017014922.1:c.2887A= XP_016870411.1:p.Arg963=
XM_017014923.1:c.3034A= XP_016870412.1:p.Arg1012=
XM_017014924.1:c.1516A= XP_016870413.1:p.Arg506=
NM_018249.6:c.3721A= MANE Select NP_060719.4:p.Arg1241=
NM_001011649.3:c.3721A= NP_001011649.1:p.Arg1241=
NR_073554.2:n.3987A=
NR_073555.2:n.3910A=
NR_073556.2:n.4117A=
NR_073557.2:n.3990A=
NR_073558.2:n.3987A=
NM_001272039.2:c.3031A= NP_001258968.1:p.Arg1011=