Canonical Allele Identifier: CA1876636240
Gene: CDK5RAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120439504A= , CM000671.2:g.120439504A= GRCh38
NC_000009.11:g.123201782A= , CM000671.1:g.123201782A= GRCh37
NC_000009.10:g.122241603A= NCBI36
NG_008999.1:g.145656T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360822.8:c.2927T= ENSP00000354065.4:p.Leu976=
ENST00000416449.6:c.3521T= ENSP00000400395.2:p.Leu1174=
ENST00000479584.2:n.1864T=
ENST00000684780.1:n.3907T=
ENST00000685866.1:c.*1444T= ENSP00000509484.1:n.*1444T=
ENST00000686376.1:c.3697T= ENSP00000510021.1:n.3697T=
ENST00000686842.1:n.7171T=
ENST00000687279.1:c.3614T= ENSP00000508692.1:p.Leu1205=
ENST00000687311.1:n.3580T=
ENST00000687633.1:c.3518T= ENSP00000510289.1:p.Leu1173=
ENST00000688923.1:n.2989T=
ENST00000689688.1:c.3617T= ENSP00000510155.1:p.Leu1206=
ENST00000690646.1:c.3521T= ENSP00000510383.1:p.Leu1174=
ENST00000690814.1:c.*793T= ENSP00000508792.1:n.*793T=
ENST00000691504.1:n.3511T=
ENST00000692155.1:c.3697T= ENSP00000510290.1:n.3697T=
ENST00000692746.1:n.3524T=
ENST00000693386.1:c.3521T= ENSP00000510003.1:p.Leu1174=
ENST00000693433.1:n.3511T=
ENST00000693714.1:n.3564T=
ENST00000693728.1:c.3521T= ENSP00000510580.1:p.Leu1174=
ENST00000349780.9:c.3617T= MANE Select ENSP00000343818.4:p.Leu1206=
ENST00000349780.8:c.3617T= ENSP00000343818.4:p.Leu1206=
ENST00000360190.8:c.3617T= ENSP00000353317.4:p.Leu1206=
ENST00000360822.7:c.2927T= ENSP00000354065.4:p.Leu976=
ENST00000416449.5:c.1799T= ENSP00000400395.1:p.Leu600=
ENST00000425647.1:c.647T= ENSP00000409941.1:p.Leu216=
ENST00000473282.6:c.*2441T= ENSP00000419265.1:n.*2441T=
ENST00000480112.5:c.*1444T= ENSP00000418418.1:n.*1444T=
ENST00000483412.5:n.2925T=
NM_001011649.2:c.3617T= NP_001011649.1:p.Leu1206=
NM_001272039.1:c.2927T= NP_001258968.1:p.Leu976=
NM_018249.5:c.3617T= NP_060719.4:p.Leu1206=
NR_073554.1:n.3886T=
NR_073555.1:n.3809T=
NR_073556.1:n.4016T=
NR_073557.1:n.3889T=
NR_073558.1:n.3886T=
XM_006717182.1:c.3521T= XP_006717245.1:p.Leu1174=
XM_006717185.1:c.2930T= XP_006717248.1:p.Leu977=
XM_011518860.1:c.3614T= XP_011517162.1:p.Leu1205=
XM_011518861.1:c.3614T= XP_011517163.1:p.Leu1205=
XM_017014921.1:c.3518T= XP_016870410.1:p.Leu1173=
XM_017014922.1:c.2783T= XP_016870411.1:p.Leu928=
XM_017014923.1:c.2930T= XP_016870412.1:p.Leu977=
XM_017014924.1:c.1412T= XP_016870413.1:p.Leu471=
NM_018249.6:c.3617T= MANE Select NP_060719.4:p.Leu1206=
NM_001011649.3:c.3617T= NP_001011649.1:p.Leu1206=
NR_073554.2:n.3883T=
NR_073555.2:n.3806T=
NR_073556.2:n.4013T=
NR_073557.2:n.3886T=
NR_073558.2:n.3883T=
NM_001272039.2:c.2927T= NP_001258968.1:p.Leu976=