Canonical Allele Identifier: CA1876636237
Gene: CDK5RAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120439497T= , CM000671.2:g.120439497T= GRCh38
NC_000009.11:g.123201775T= , CM000671.1:g.123201775T= GRCh37
NC_000009.10:g.122241596T= NCBI36
NG_008999.1:g.145663A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360822.8:c.2934A= ENSP00000354065.4:p.Glu978=
ENST00000416449.6:c.3528A= ENSP00000400395.2:p.Glu1176=
ENST00000479584.2:n.1871A=
ENST00000684780.1:n.3914A=
ENST00000685866.1:c.*1451A= ENSP00000509484.1:n.*1451A=
ENST00000686376.1:c.3704A= ENSP00000510021.1:n.3704A=
ENST00000686842.1:n.7178A=
ENST00000687279.1:c.3621A= ENSP00000508692.1:p.Glu1207=
ENST00000687311.1:n.3587A=
ENST00000687633.1:c.3525A= ENSP00000510289.1:p.Glu1175=
ENST00000688923.1:n.2996A=
ENST00000689688.1:c.3624A= ENSP00000510155.1:p.Glu1208=
ENST00000690646.1:c.3528A= ENSP00000510383.1:p.Glu1176=
ENST00000690814.1:c.*800A= ENSP00000508792.1:n.*800A=
ENST00000691504.1:n.3518A=
ENST00000692155.1:c.3704A= ENSP00000510290.1:n.3704A=
ENST00000692746.1:n.3531A=
ENST00000693386.1:c.3528A= ENSP00000510003.1:p.Glu1176=
ENST00000693433.1:n.3518A=
ENST00000693714.1:n.3571A=
ENST00000693728.1:c.3528A= ENSP00000510580.1:p.Glu1176=
ENST00000349780.9:c.3624A= MANE Select ENSP00000343818.4:p.Glu1208=
ENST00000349780.8:c.3624A= ENSP00000343818.4:p.Glu1208=
ENST00000360190.8:c.3624A= ENSP00000353317.4:p.Glu1208=
ENST00000360822.7:c.2934A= ENSP00000354065.4:p.Glu978=
ENST00000416449.5:c.1806A= ENSP00000400395.1:p.Glu602=
ENST00000425647.1:c.654A= ENSP00000409941.1:p.Glu218=
ENST00000473282.6:c.*2448A= ENSP00000419265.1:n.*2448A=
ENST00000480112.5:c.*1451A= ENSP00000418418.1:n.*1451A=
ENST00000483412.5:n.2932A=
NM_001011649.2:c.3624A= NP_001011649.1:p.Glu1208=
NM_001272039.1:c.2934A= NP_001258968.1:p.Glu978=
NM_018249.5:c.3624A= NP_060719.4:p.Glu1208=
NR_073554.1:n.3893A=
NR_073555.1:n.3816A=
NR_073556.1:n.4023A=
NR_073557.1:n.3896A=
NR_073558.1:n.3893A=
XM_006717182.1:c.3528A= XP_006717245.1:p.Glu1176=
XM_006717185.1:c.2937A= XP_006717248.1:p.Glu979=
XM_011518860.1:c.3621A= XP_011517162.1:p.Glu1207=
XM_011518861.1:c.3621A= XP_011517163.1:p.Glu1207=
XM_017014921.1:c.3525A= XP_016870410.1:p.Glu1175=
XM_017014922.1:c.2790A= XP_016870411.1:p.Glu930=
XM_017014923.1:c.2937A= XP_016870412.1:p.Glu979=
XM_017014924.1:c.1419A= XP_016870413.1:p.Glu473=
NM_018249.6:c.3624A= MANE Select NP_060719.4:p.Glu1208=
NM_001011649.3:c.3624A= NP_001011649.1:p.Glu1208=
NR_073554.2:n.3890A=
NR_073555.2:n.3813A=
NR_073556.2:n.4020A=
NR_073557.2:n.3893A=
NR_073558.2:n.3890A=
NM_001272039.2:c.2934A= NP_001258968.1:p.Glu978=