Canonical Allele Identifier: CA374721121

Gene: CDK5RAP2

Linked Data

• MyVariant Identifiers: chr9:g.123201773T>C (hg19) ; chr9:g.120439495T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120439495T>C , CM000671.2:g.120439495T>C	GRCh38
NC_000009.11:g.123201773T>C , CM000671.1:g.123201773T>C	GRCh37
NC_000009.10:g.122241594T>C	NCBI36
NG_008999.1:g.145665A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360822.8:c.2936A>G	ENSP00000354065.4:p.Gln979Arg
ENST00000416449.6:c.3530A>G	ENSP00000400395.2:p.Gln1177Arg
ENST00000479584.2:n.1873A>G
ENST00000684780.1:n.3916A>G
ENST00000685866.1:c.*1453A>G	ENSP00000509484.1:n.*1453A>G
ENST00000686376.1:c.3706A>G	ENSP00000510021.1:n.3706A>G
ENST00000686842.1:n.7180A>G
ENST00000687279.1:c.3623A>G	ENSP00000508692.1:p.Gln1208Arg
ENST00000687311.1:n.3589A>G
ENST00000687633.1:c.3527A>G	ENSP00000510289.1:p.Gln1176Arg
ENST00000688923.1:n.2998A>G
ENST00000689688.1:c.3626A>G	ENSP00000510155.1:p.Gln1209Arg
ENST00000690646.1:c.3530A>G	ENSP00000510383.1:p.Gln1177Arg
ENST00000690814.1:c.*802A>G	ENSP00000508792.1:n.*802A>G
ENST00000691504.1:n.3520A>G
ENST00000692155.1:c.3706A>G	ENSP00000510290.1:n.3706A>G
ENST00000692746.1:n.3533A>G
ENST00000693386.1:c.3530A>G	ENSP00000510003.1:p.Gln1177Arg
ENST00000693433.1:n.3520A>G
ENST00000693714.1:n.3573A>G
ENST00000693728.1:c.3530A>G	ENSP00000510580.1:p.Gln1177Arg
ENST00000349780.9:c.3626A>G MANE Select	ENSP00000343818.4:p.Gln1209Arg
ENST00000349780.8:c.3626A>G	ENSP00000343818.4:p.Gln1209Arg
ENST00000360190.8:c.3626A>G	ENSP00000353317.4:p.Gln1209Arg
ENST00000360822.7:c.2936A>G	ENSP00000354065.4:p.Gln979Arg
ENST00000416449.5:c.1808A>G	ENSP00000400395.1:p.Gln603Arg
ENST00000425647.1:c.656A>G	ENSP00000409941.1:p.Gln219Arg
ENST00000473282.6:c.*2450A>G	ENSP00000419265.1:n.*2450A>G
ENST00000480112.5:c.*1453A>G	ENSP00000418418.1:n.*1453A>G
ENST00000483412.5:n.2934A>G
NM_001011649.2:c.3626A>G	NP_001011649.1:p.Gln1209Arg
NM_001272039.1:c.2936A>G	NP_001258968.1:p.Gln979Arg
NM_018249.5:c.3626A>G	NP_060719.4:p.Gln1209Arg
NR_073554.1:n.3895A>G
NR_073555.1:n.3818A>G
NR_073556.1:n.4025A>G
NR_073557.1:n.3898A>G
NR_073558.1:n.3895A>G
XM_006717182.1:c.3530A>G	XP_006717245.1:p.Gln1177Arg
XM_006717185.1:c.2939A>G	XP_006717248.1:p.Gln980Arg
XM_011518860.1:c.3623A>G	XP_011517162.1:p.Gln1208Arg
XM_011518861.1:c.3623A>G	XP_011517163.1:p.Gln1208Arg
XM_017014921.1:c.3527A>G	XP_016870410.1:p.Gln1176Arg
XM_017014922.1:c.2792A>G	XP_016870411.1:p.Gln931Arg
XM_017014923.1:c.2939A>G	XP_016870412.1:p.Gln980Arg
XM_017014924.1:c.1421A>G	XP_016870413.1:p.Gln474Arg
NM_018249.6:c.3626A>G MANE Select	NP_060719.4:p.Gln1209Arg
NM_001011649.3:c.3626A>G	NP_001011649.1:p.Gln1209Arg
NR_073554.2:n.3892A>G
NR_073555.2:n.3815A>G
NR_073556.2:n.4022A>G
NR_073557.2:n.3895A>G
NR_073558.2:n.3892A>G
NM_001272039.2:c.2936A>G	NP_001258968.1:p.Gln979Arg