Canonical Allele Identifier: CA374721101

Gene: CDK5RAP2

Linked Data

• MyVariant Identifiers: chr9:g.123201765T>A (hg19) ; chr9:g.120439487T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120439487T>A , CM000671.2:g.120439487T>A	GRCh38
NC_000009.11:g.123201765T>A , CM000671.1:g.123201765T>A	GRCh37
NC_000009.10:g.122241586T>A	NCBI36
NG_008999.1:g.145673A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360822.8:c.2944A>T	ENSP00000354065.4:p.Lys982Ter
ENST00000416449.6:c.3538A>T	ENSP00000400395.2:p.Lys1180Ter
ENST00000479584.2:n.1881A>T
ENST00000684780.1:n.3924A>T
ENST00000685866.1:c.*1461A>T	ENSP00000509484.1:n.*1461A>T
ENST00000686376.1:c.3714A>T	ENSP00000510021.1:n.3714A>T
ENST00000686842.1:n.7188A>T
ENST00000687279.1:c.3631A>T	ENSP00000508692.1:p.Lys1211Ter
ENST00000687311.1:n.3597A>T
ENST00000687633.1:c.3535A>T	ENSP00000510289.1:p.Lys1179Ter
ENST00000688923.1:n.3006A>T
ENST00000689688.1:c.3634A>T	ENSP00000510155.1:p.Lys1212Ter
ENST00000690646.1:c.3538A>T	ENSP00000510383.1:p.Lys1180Ter
ENST00000690814.1:c.*810A>T	ENSP00000508792.1:n.*810A>T
ENST00000691504.1:n.3528A>T
ENST00000692155.1:c.3714A>T	ENSP00000510290.1:n.3714A>T
ENST00000692746.1:n.3541A>T
ENST00000693386.1:c.3538A>T	ENSP00000510003.1:p.Lys1180Ter
ENST00000693433.1:n.3528A>T
ENST00000693714.1:n.3581A>T
ENST00000693728.1:c.3538A>T	ENSP00000510580.1:p.Lys1180Ter
ENST00000349780.9:c.3634A>T MANE Select	ENSP00000343818.4:p.Lys1212Ter
ENST00000349780.8:c.3634A>T	ENSP00000343818.4:p.Lys1212Ter
ENST00000360190.8:c.3634A>T	ENSP00000353317.4:p.Lys1212Ter
ENST00000360822.7:c.2944A>T	ENSP00000354065.4:p.Lys982Ter
ENST00000416449.5:c.1816A>T	ENSP00000400395.1:p.Lys606Ter
ENST00000425647.1:c.664A>T	ENSP00000409941.1:p.Lys222Ter
ENST00000473282.6:c.*2458A>T	ENSP00000419265.1:n.*2458A>T
ENST00000480112.5:c.*1461A>T	ENSP00000418418.1:n.*1461A>T
ENST00000483412.5:n.2942A>T
NM_001011649.2:c.3634A>T	NP_001011649.1:p.Lys1212Ter
NM_001272039.1:c.2944A>T	NP_001258968.1:p.Lys982Ter
NM_018249.5:c.3634A>T	NP_060719.4:p.Lys1212Ter
NR_073554.1:n.3903A>T
NR_073555.1:n.3826A>T
NR_073556.1:n.4033A>T
NR_073557.1:n.3906A>T
NR_073558.1:n.3903A>T
XM_006717182.1:c.3538A>T	XP_006717245.1:p.Lys1180Ter
XM_006717185.1:c.2947A>T	XP_006717248.1:p.Lys983Ter
XM_011518860.1:c.3631A>T	XP_011517162.1:p.Lys1211Ter
XM_011518861.1:c.3631A>T	XP_011517163.1:p.Lys1211Ter
XM_017014921.1:c.3535A>T	XP_016870410.1:p.Lys1179Ter
XM_017014922.1:c.2800A>T	XP_016870411.1:p.Lys934Ter
XM_017014923.1:c.2947A>T	XP_016870412.1:p.Lys983Ter
XM_017014924.1:c.1429A>T	XP_016870413.1:p.Lys477Ter
NM_018249.6:c.3634A>T MANE Select	NP_060719.4:p.Lys1212Ter
NM_001011649.3:c.3634A>T	NP_001011649.1:p.Lys1212Ter
NR_073554.2:n.3900A>T
NR_073555.2:n.3823A>T
NR_073556.2:n.4030A>T
NR_073557.2:n.3903A>T
NR_073558.2:n.3900A>T
NM_001272039.2:c.2944A>T	NP_001258968.1:p.Lys982Ter