Canonical Allele Identifier: CA374721112

Gene: CDK5RAP2

Linked Data

• MyVariant Identifiers: chr9:g.123201770T>G (hg19) ; chr9:g.120439492T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120439492T>G , CM000671.2:g.120439492T>G	GRCh38
NC_000009.11:g.123201770T>G , CM000671.1:g.123201770T>G	GRCh37
NC_000009.10:g.122241591T>G	NCBI36
NG_008999.1:g.145668A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360822.8:c.2939A>C	ENSP00000354065.4:p.Glu980Ala
ENST00000416449.6:c.3533A>C	ENSP00000400395.2:p.Glu1178Ala
ENST00000479584.2:n.1876A>C
ENST00000684780.1:n.3919A>C
ENST00000685866.1:c.*1456A>C	ENSP00000509484.1:n.*1456A>C
ENST00000686376.1:c.3709A>C	ENSP00000510021.1:n.3709A>C
ENST00000686842.1:n.7183A>C
ENST00000687279.1:c.3626A>C	ENSP00000508692.1:p.Glu1209Ala
ENST00000687311.1:n.3592A>C
ENST00000687633.1:c.3530A>C	ENSP00000510289.1:p.Glu1177Ala
ENST00000688923.1:n.3001A>C
ENST00000689688.1:c.3629A>C	ENSP00000510155.1:p.Glu1210Ala
ENST00000690646.1:c.3533A>C	ENSP00000510383.1:p.Glu1178Ala
ENST00000690814.1:c.*805A>C	ENSP00000508792.1:n.*805A>C
ENST00000691504.1:n.3523A>C
ENST00000692155.1:c.3709A>C	ENSP00000510290.1:n.3709A>C
ENST00000692746.1:n.3536A>C
ENST00000693386.1:c.3533A>C	ENSP00000510003.1:p.Glu1178Ala
ENST00000693433.1:n.3523A>C
ENST00000693714.1:n.3576A>C
ENST00000693728.1:c.3533A>C	ENSP00000510580.1:p.Glu1178Ala
ENST00000349780.9:c.3629A>C MANE Select	ENSP00000343818.4:p.Glu1210Ala
ENST00000349780.8:c.3629A>C	ENSP00000343818.4:p.Glu1210Ala
ENST00000360190.8:c.3629A>C	ENSP00000353317.4:p.Glu1210Ala
ENST00000360822.7:c.2939A>C	ENSP00000354065.4:p.Glu980Ala
ENST00000416449.5:c.1811A>C	ENSP00000400395.1:p.Glu604Ala
ENST00000425647.1:c.659A>C	ENSP00000409941.1:p.Glu220Ala
ENST00000473282.6:c.*2453A>C	ENSP00000419265.1:n.*2453A>C
ENST00000480112.5:c.*1456A>C	ENSP00000418418.1:n.*1456A>C
ENST00000483412.5:n.2937A>C
NM_001011649.2:c.3629A>C	NP_001011649.1:p.Glu1210Ala
NM_001272039.1:c.2939A>C	NP_001258968.1:p.Glu980Ala
NM_018249.5:c.3629A>C	NP_060719.4:p.Glu1210Ala
NR_073554.1:n.3898A>C
NR_073555.1:n.3821A>C
NR_073556.1:n.4028A>C
NR_073557.1:n.3901A>C
NR_073558.1:n.3898A>C
XM_006717182.1:c.3533A>C	XP_006717245.1:p.Glu1178Ala
XM_006717185.1:c.2942A>C	XP_006717248.1:p.Glu981Ala
XM_011518860.1:c.3626A>C	XP_011517162.1:p.Glu1209Ala
XM_011518861.1:c.3626A>C	XP_011517163.1:p.Glu1209Ala
XM_017014921.1:c.3530A>C	XP_016870410.1:p.Glu1177Ala
XM_017014922.1:c.2795A>C	XP_016870411.1:p.Glu932Ala
XM_017014923.1:c.2942A>C	XP_016870412.1:p.Glu981Ala
XM_017014924.1:c.1424A>C	XP_016870413.1:p.Glu475Ala
NM_018249.6:c.3629A>C MANE Select	NP_060719.4:p.Glu1210Ala
NM_001011649.3:c.3629A>C	NP_001011649.1:p.Glu1210Ala
NR_073554.2:n.3895A>C
NR_073555.2:n.3818A>C
NR_073556.2:n.4025A>C
NR_073557.2:n.3898A>C
NR_073558.2:n.3895A>C
NM_001272039.2:c.2939A>C	NP_001258968.1:p.Glu980Ala