Canonical Allele Identifier: CA1876636201
Gene: CDK5RAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120439408G= , CM000671.2:g.120439408G= GRCh38
NC_000009.11:g.123201686G= , CM000671.1:g.123201686G= GRCh37
NC_000009.10:g.122241507G= NCBI36
NG_008999.1:g.145752C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360822.8:c.3023C= ENSP00000354065.4:p.Ser1008=
ENST00000416449.6:c.3617C= ENSP00000400395.2:p.Ser1206=
ENST00000479584.2:n.1960C=
ENST00000684780.1:n.4003C=
ENST00000685866.1:c.*1540C= ENSP00000509484.1:n.*1540C=
ENST00000686376.1:c.3793C= ENSP00000510021.1:n.3793C=
ENST00000686842.1:n.7267C=
ENST00000687279.1:c.3710C= ENSP00000508692.1:p.Ser1237=
ENST00000687311.1:n.3676C=
ENST00000687633.1:c.3614C= ENSP00000510289.1:p.Ser1205=
ENST00000688923.1:n.3085C=
ENST00000689688.1:c.3713C= ENSP00000510155.1:p.Ser1238=
ENST00000690646.1:c.3617C= ENSP00000510383.1:p.Ser1206=
ENST00000690814.1:c.*889C= ENSP00000508792.1:n.*889C=
ENST00000691504.1:n.3607C=
ENST00000692155.1:c.3793C= ENSP00000510290.1:n.3793C=
ENST00000692746.1:n.3620C=
ENST00000693386.1:c.3617C= ENSP00000510003.1:p.Ser1206=
ENST00000693433.1:n.3607C=
ENST00000693714.1:n.3660C=
ENST00000693728.1:c.3617C= ENSP00000510580.1:p.Ser1206=
ENST00000349780.9:c.3713C= MANE Select ENSP00000343818.4:p.Ser1238=
ENST00000349780.8:c.3713C= ENSP00000343818.4:p.Ser1238=
ENST00000360190.8:c.3713C= ENSP00000353317.4:p.Ser1238=
ENST00000360822.7:c.3023C= ENSP00000354065.4:p.Ser1008=
ENST00000416449.5:c.1895C= ENSP00000400395.1:p.Ser632=
ENST00000425647.1:c.743C= ENSP00000409941.1:p.Ser248=
ENST00000473282.6:c.*2537C= ENSP00000419265.1:n.*2537C=
ENST00000480112.5:c.*1540C= ENSP00000418418.1:n.*1540C=
ENST00000483412.5:n.3021C=
NM_001011649.2:c.3713C= NP_001011649.1:p.Ser1238=
NM_001272039.1:c.3023C= NP_001258968.1:p.Ser1008=
NM_018249.5:c.3713C= NP_060719.4:p.Ser1238=
NR_073554.1:n.3982C=
NR_073555.1:n.3905C=
NR_073556.1:n.4112C=
NR_073557.1:n.3985C=
NR_073558.1:n.3982C=
XM_006717182.1:c.3617C= XP_006717245.1:p.Ser1206=
XM_006717185.1:c.3026C= XP_006717248.1:p.Ser1009=
XM_011518860.1:c.3710C= XP_011517162.1:p.Ser1237=
XM_011518861.1:c.3710C= XP_011517163.1:p.Ser1237=
XM_017014921.1:c.3614C= XP_016870410.1:p.Ser1205=
XM_017014922.1:c.2879C= XP_016870411.1:p.Ser960=
XM_017014923.1:c.3026C= XP_016870412.1:p.Ser1009=
XM_017014924.1:c.1508C= XP_016870413.1:p.Ser503=
NM_018249.6:c.3713C= MANE Select NP_060719.4:p.Ser1238=
NM_001011649.3:c.3713C= NP_001011649.1:p.Ser1238=
NR_073554.2:n.3979C=
NR_073555.2:n.3902C=
NR_073556.2:n.4109C=
NR_073557.2:n.3982C=
NR_073558.2:n.3979C=
NM_001272039.2:c.3023C= NP_001258968.1:p.Ser1008=