Canonical Allele Identifier: CA374721118

Gene: CDK5RAP2

Linked Data

• MyVariant Identifiers: chr9:g.123201772C>A (hg19) ; chr9:g.120439494C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120439494C>A , CM000671.2:g.120439494C>A	GRCh38
NC_000009.11:g.123201772C>A , CM000671.1:g.123201772C>A	GRCh37
NC_000009.10:g.122241593C>A	NCBI36
NG_008999.1:g.145666G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360822.8:c.2937G>T	ENSP00000354065.4:p.Gln979His
ENST00000416449.6:c.3531G>T	ENSP00000400395.2:p.Gln1177His
ENST00000479584.2:n.1874G>T
ENST00000684780.1:n.3917G>T
ENST00000685866.1:c.*1454G>T	ENSP00000509484.1:n.*1454G>T
ENST00000686376.1:c.3707G>T	ENSP00000510021.1:n.3707G>T
ENST00000686842.1:n.7181G>T
ENST00000687279.1:c.3624G>T	ENSP00000508692.1:p.Gln1208His
ENST00000687311.1:n.3590G>T
ENST00000687633.1:c.3528G>T	ENSP00000510289.1:p.Gln1176His
ENST00000688923.1:n.2999G>T
ENST00000689688.1:c.3627G>T	ENSP00000510155.1:p.Gln1209His
ENST00000690646.1:c.3531G>T	ENSP00000510383.1:p.Gln1177His
ENST00000690814.1:c.*803G>T	ENSP00000508792.1:n.*803G>T
ENST00000691504.1:n.3521G>T
ENST00000692155.1:c.3707G>T	ENSP00000510290.1:n.3707G>T
ENST00000692746.1:n.3534G>T
ENST00000693386.1:c.3531G>T	ENSP00000510003.1:p.Gln1177His
ENST00000693433.1:n.3521G>T
ENST00000693714.1:n.3574G>T
ENST00000693728.1:c.3531G>T	ENSP00000510580.1:p.Gln1177His
ENST00000349780.9:c.3627G>T MANE Select	ENSP00000343818.4:p.Gln1209His
ENST00000349780.8:c.3627G>T	ENSP00000343818.4:p.Gln1209His
ENST00000360190.8:c.3627G>T	ENSP00000353317.4:p.Gln1209His
ENST00000360822.7:c.2937G>T	ENSP00000354065.4:p.Gln979His
ENST00000416449.5:c.1809G>T	ENSP00000400395.1:p.Gln603His
ENST00000425647.1:c.657G>T	ENSP00000409941.1:p.Gln219His
ENST00000473282.6:c.*2451G>T	ENSP00000419265.1:n.*2451G>T
ENST00000480112.5:c.*1454G>T	ENSP00000418418.1:n.*1454G>T
ENST00000483412.5:n.2935G>T
NM_001011649.2:c.3627G>T	NP_001011649.1:p.Gln1209His
NM_001272039.1:c.2937G>T	NP_001258968.1:p.Gln979His
NM_018249.5:c.3627G>T	NP_060719.4:p.Gln1209His
NR_073554.1:n.3896G>T
NR_073555.1:n.3819G>T
NR_073556.1:n.4026G>T
NR_073557.1:n.3899G>T
NR_073558.1:n.3896G>T
XM_006717182.1:c.3531G>T	XP_006717245.1:p.Gln1177His
XM_006717185.1:c.2940G>T	XP_006717248.1:p.Gln980His
XM_011518860.1:c.3624G>T	XP_011517162.1:p.Gln1208His
XM_011518861.1:c.3624G>T	XP_011517163.1:p.Gln1208His
XM_017014921.1:c.3528G>T	XP_016870410.1:p.Gln1176His
XM_017014922.1:c.2793G>T	XP_016870411.1:p.Gln931His
XM_017014923.1:c.2940G>T	XP_016870412.1:p.Gln980His
XM_017014924.1:c.1422G>T	XP_016870413.1:p.Gln474His
NM_018249.6:c.3627G>T MANE Select	NP_060719.4:p.Gln1209His
NM_001011649.3:c.3627G>T	NP_001011649.1:p.Gln1209His
NR_073554.2:n.3893G>T
NR_073555.2:n.3816G>T
NR_073556.2:n.4023G>T
NR_073557.2:n.3896G>T
NR_073558.2:n.3893G>T
NM_001272039.2:c.2937G>T	NP_001258968.1:p.Gln979His