Canonical Allele Identifier: CA2241859227

Gene: CDK10

Linked Data

• dbSNP Id: rs2060615446
• gnomAD v4: 16-89694629-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89694629A>G , CM000678.2:g.89694629A>G	GRCh38
NC_000016.9:g.89761037A>G , CM000678.1:g.89761037A>G	GRCh37
NC_000016.8:g.88288538A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000353379.12:c.669-36A>G MANE Select	ENSP00000338673.7:n.669-36A>G
ENST00000331006.12:c.528-36A>G	ENSP00000329957.8:n.528-36A>G
ENST00000353379.11:c.669-36A>G	ENSP00000338673.7:n.669-36A>G
ENST00000472018.5:n.1456-36A>G
ENST00000505473.5:c.456-36A>G	ENSP00000424415.1:n.456-36A>G
ENST00000505733.5:n.761-36A>G
ENST00000510811.6:c.*467-36A>G	ENSP00000455976.1:n.*467-36A>G
ENST00000564192.5:c.516A>G	ENSP00000457055.1:p.Arg172=
ENST00000565470.1:c.50-302A>G
ENST00000617879.1:c.456-36A>G	ENSP00000484357.1:n.456-36A>G
NM_001098533.2:c.456-36A>G	NP_001092003.2:n.456-36A>G
NM_001160367.1:c.456-36A>G	NP_001153839.1:n.456-36A>G
NM_052987.3:c.456-36A>G	NP_443713.2:n.456-36A>G
NM_052988.4:c.669-36A>G	NP_443714.3:n.669-36A>G
NR_027702.1:n.639-36A>G
NR_027703.1:n.639-36A>G
XM_006721308.1:c.669-36A>G	XP_006721371.1:n.669-36A>G
XM_006721310.1:c.669-36A>G	XP_006721373.1:n.669-36A>G
XM_011523405.1:c.729A>G	XP_011521707.1:p.Arg243=
XM_011523406.1:c.729A>G	XP_011521708.1:p.Arg243=
XM_011523407.1:c.729A>G	XP_011521709.1:p.Arg243=
XM_011523408.1:c.729A>G	XP_011521710.1:p.Arg243=
XM_011523409.1:c.618A>G	XP_011521711.1:p.Arg206=
XM_011523410.1:c.516A>G	XP_011521712.1:p.Arg172=
XM_011523411.1:c.516A>G	XP_011521713.1:p.Arg172=
XM_011523412.1:c.516A>G	XP_011521714.1:p.Arg172=
XM_011523413.1:c.516A>G	XP_011521715.1:p.Arg172=
XM_011523414.1:c.516A>G	XP_011521716.1:p.Arg172=
XM_011523415.1:c.516A>G	XP_011521717.1:p.Arg172=
XM_011523416.1:c.516A>G	XP_011521718.1:p.Arg172=
XR_933471.1:n.2686-36A>G
XM_006721308.3:c.669-36A>G	XP_006721371.1:n.669-36A>G
XM_006721310.3:c.669-36A>G	XP_006721373.1:n.669-36A>G
XM_011523405.3:c.729A>G	XP_011521707.1:p.Arg243=
XM_011523406.3:c.729A>G	XP_011521708.1:p.Arg243=
XM_011523407.3:c.729A>G	XP_011521709.1:p.Arg243=
XM_011523408.3:c.729A>G	XP_011521710.1:p.Arg243=
XM_011523410.2:c.516A>G	XP_011521712.1:p.Arg172=
XM_011523411.2:c.516A>G	XP_011521713.1:p.Arg172=
XM_011523413.2:c.516A>G	XP_011521715.1:p.Arg172=
XM_011523414.2:c.516A>G	XP_011521716.1:p.Arg172=
XM_011523415.3:c.516A>G	XP_011521717.1:p.Arg172=
XM_011523416.2:c.516A>G	XP_011521718.1:p.Arg172=
XM_017023806.1:c.618A>G	XP_016879295.1:p.Arg206=
XM_017023807.2:c.669-36A>G	XP_016879296.1:n.669-36A>G
XM_017023808.1:c.456-36A>G	XP_016879297.1:n.456-36A>G
XM_017023809.2:c.456-36A>G	XP_016879298.1:n.456-36A>G
XM_017023810.1:c.456-36A>G	XP_016879299.1:n.456-36A>G
NM_052988.5:c.669-36A>G MANE Select	NP_443714.3:n.669-36A>G
NM_001098533.3:c.456-36A>G	NP_001092003.2:n.456-36A>G
NM_001160367.2:c.456-36A>G	NP_001153839.1:n.456-36A>G
NM_052987.4:c.456-36A>G	NP_443713.2:n.456-36A>G
NR_027702.2:n.618-36A>G
NR_027703.2:n.618-36A>G