Canonical Allele Identifier: CA1876636204
Gene: CDK5RAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120439426T= , CM000671.2:g.120439426T= GRCh38
NC_000009.11:g.123201704T= , CM000671.1:g.123201704T= GRCh37
NC_000009.10:g.122241525T= NCBI36
NG_008999.1:g.145734A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360822.8:c.3005A= ENSP00000354065.4:p.Asn1002=
ENST00000416449.6:c.3599A= ENSP00000400395.2:p.Asn1200=
ENST00000479584.2:n.1942A=
ENST00000684780.1:n.3985A=
ENST00000685866.1:c.*1522A= ENSP00000509484.1:n.*1522A=
ENST00000686376.1:c.3775A= ENSP00000510021.1:n.3775A=
ENST00000686842.1:n.7249A=
ENST00000687279.1:c.3692A= ENSP00000508692.1:p.Asn1231=
ENST00000687311.1:n.3658A=
ENST00000687633.1:c.3596A= ENSP00000510289.1:p.Asn1199=
ENST00000688923.1:n.3067A=
ENST00000689688.1:c.3695A= ENSP00000510155.1:p.Asn1232=
ENST00000690646.1:c.3599A= ENSP00000510383.1:p.Asn1200=
ENST00000690814.1:c.*871A= ENSP00000508792.1:n.*871A=
ENST00000691504.1:n.3589A=
ENST00000692155.1:c.3775A= ENSP00000510290.1:n.3775A=
ENST00000692746.1:n.3602A=
ENST00000693386.1:c.3599A= ENSP00000510003.1:p.Asn1200=
ENST00000693433.1:n.3589A=
ENST00000693714.1:n.3642A=
ENST00000693728.1:c.3599A= ENSP00000510580.1:p.Asn1200=
ENST00000349780.9:c.3695A= MANE Select ENSP00000343818.4:p.Asn1232=
ENST00000349780.8:c.3695A= ENSP00000343818.4:p.Asn1232=
ENST00000360190.8:c.3695A= ENSP00000353317.4:p.Asn1232=
ENST00000360822.7:c.3005A= ENSP00000354065.4:p.Asn1002=
ENST00000416449.5:c.1877A= ENSP00000400395.1:p.Asn626=
ENST00000425647.1:c.725A= ENSP00000409941.1:p.Asn242=
ENST00000473282.6:c.*2519A= ENSP00000419265.1:n.*2519A=
ENST00000480112.5:c.*1522A= ENSP00000418418.1:n.*1522A=
ENST00000483412.5:n.3003A=
NM_001011649.2:c.3695A= NP_001011649.1:p.Asn1232=
NM_001272039.1:c.3005A= NP_001258968.1:p.Asn1002=
NM_018249.5:c.3695A= NP_060719.4:p.Asn1232=
NR_073554.1:n.3964A=
NR_073555.1:n.3887A=
NR_073556.1:n.4094A=
NR_073557.1:n.3967A=
NR_073558.1:n.3964A=
XM_006717182.1:c.3599A= XP_006717245.1:p.Asn1200=
XM_006717185.1:c.3008A= XP_006717248.1:p.Asn1003=
XM_011518860.1:c.3692A= XP_011517162.1:p.Asn1231=
XM_011518861.1:c.3692A= XP_011517163.1:p.Asn1231=
XM_017014921.1:c.3596A= XP_016870410.1:p.Asn1199=
XM_017014922.1:c.2861A= XP_016870411.1:p.Asn954=
XM_017014923.1:c.3008A= XP_016870412.1:p.Asn1003=
XM_017014924.1:c.1490A= XP_016870413.1:p.Asn497=
NM_018249.6:c.3695A= MANE Select NP_060719.4:p.Asn1232=
NM_001011649.3:c.3695A= NP_001011649.1:p.Asn1232=
NR_073554.2:n.3961A=
NR_073555.2:n.3884A=
NR_073556.2:n.4091A=
NR_073557.2:n.3964A=
NR_073558.2:n.3961A=
NM_001272039.2:c.3005A= NP_001258968.1:p.Asn1002=