Canonical Allele Identifier: CA1876636198
Gene: CDK5RAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120439403G= , CM000671.2:g.120439403G= GRCh38
NC_000009.11:g.123201681G= , CM000671.1:g.123201681G= GRCh37
NC_000009.10:g.122241502G= NCBI36
NG_008999.1:g.145757C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360822.8:c.3028C= ENSP00000354065.4:p.Pro1010=
ENST00000416449.6:c.3622C= ENSP00000400395.2:p.Pro1208=
ENST00000479584.2:n.1965C=
ENST00000684780.1:n.4008C=
ENST00000685866.1:c.*1545C= ENSP00000509484.1:n.*1545C=
ENST00000686376.1:c.3798C= ENSP00000510021.1:n.3798C=
ENST00000686842.1:n.7272C=
ENST00000687279.1:c.3715C= ENSP00000508692.1:p.Pro1239=
ENST00000687311.1:n.3681C=
ENST00000687633.1:c.3619C= ENSP00000510289.1:p.Pro1207=
ENST00000688923.1:n.3090C=
ENST00000689688.1:c.3718C= ENSP00000510155.1:p.Pro1240=
ENST00000690646.1:c.3622C= ENSP00000510383.1:p.Pro1208=
ENST00000690814.1:c.*894C= ENSP00000508792.1:n.*894C=
ENST00000691504.1:n.3612C=
ENST00000692155.1:c.3798C= ENSP00000510290.1:n.3798C=
ENST00000692746.1:n.3625C=
ENST00000693386.1:c.3622C= ENSP00000510003.1:p.Pro1208=
ENST00000693433.1:n.3612C=
ENST00000693714.1:n.3665C=
ENST00000693728.1:c.3622C= ENSP00000510580.1:p.Pro1208=
ENST00000349780.9:c.3718C= MANE Select ENSP00000343818.4:p.Pro1240=
ENST00000349780.8:c.3718C= ENSP00000343818.4:p.Pro1240=
ENST00000360190.8:c.3718C= ENSP00000353317.4:p.Pro1240=
ENST00000360822.7:c.3028C= ENSP00000354065.4:p.Pro1010=
ENST00000416449.5:c.1900C= ENSP00000400395.1:p.Pro634=
ENST00000425647.1:c.748C= ENSP00000409941.1:p.Pro250=
ENST00000473282.6:c.*2542C= ENSP00000419265.1:n.*2542C=
ENST00000480112.5:c.*1545C= ENSP00000418418.1:n.*1545C=
ENST00000483412.5:n.3026C=
NM_001011649.2:c.3718C= NP_001011649.1:p.Pro1240=
NM_001272039.1:c.3028C= NP_001258968.1:p.Pro1010=
NM_018249.5:c.3718C= NP_060719.4:p.Pro1240=
NR_073554.1:n.3987C=
NR_073555.1:n.3910C=
NR_073556.1:n.4117C=
NR_073557.1:n.3990C=
NR_073558.1:n.3987C=
XM_006717182.1:c.3622C= XP_006717245.1:p.Pro1208=
XM_006717185.1:c.3031C= XP_006717248.1:p.Pro1011=
XM_011518860.1:c.3715C= XP_011517162.1:p.Pro1239=
XM_011518861.1:c.3715C= XP_011517163.1:p.Pro1239=
XM_017014921.1:c.3619C= XP_016870410.1:p.Pro1207=
XM_017014922.1:c.2884C= XP_016870411.1:p.Pro962=
XM_017014923.1:c.3031C= XP_016870412.1:p.Pro1011=
XM_017014924.1:c.1513C= XP_016870413.1:p.Pro505=
NM_018249.6:c.3718C= MANE Select NP_060719.4:p.Pro1240=
NM_001011649.3:c.3718C= NP_001011649.1:p.Pro1240=
NR_073554.2:n.3984C=
NR_073555.2:n.3907C=
NR_073556.2:n.4114C=
NR_073557.2:n.3987C=
NR_073558.2:n.3984C=
NM_001272039.2:c.3028C= NP_001258968.1:p.Pro1010=