Canonical Allele Identifier: CA497377641

Gene: CDK10

Linked Data

• MyVariant Identifiers: chr16:g.89761130T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89694722T>A , CM000678.2:g.89694722T>A	GRCh38
NC_000016.9:g.89761130T>A , CM000678.1:g.89761130T>A	GRCh37
NC_000016.8:g.88288631T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000353379.12:c.726T>A MANE Select	ENSP00000338673.7:p.Thr242=
ENST00000331006.12:c.585T>A	ENSP00000329957.8:p.Thr195=
ENST00000353379.11:c.726T>A	ENSP00000338673.7:p.Thr242=
ENST00000472018.5:n.1513T>A
ENST00000505473.5:c.513T>A	ENSP00000424415.1:p.Thr171=
ENST00000505733.5:n.818T>A
ENST00000510811.6:c.*524T>A	ENSP00000455976.1:n.*524T>A
ENST00000564192.5:c.609T>A	ENSP00000457055.1:p.Thr203=
ENST00000565470.1:c.50-209T>A
ENST00000617879.1:c.513T>A	ENSP00000484357.1:p.Thr171=
NM_001098533.2:c.513T>A	NP_001092003.2:p.Thr171=
NM_001160367.1:c.513T>A	NP_001153839.1:p.Thr171=
NM_052987.3:c.513T>A	NP_443713.2:p.Thr171=
NM_052988.4:c.726T>A	NP_443714.3:p.Thr242=
NR_027702.1:n.696T>A
NR_027703.1:n.696T>A
XM_006721308.1:c.726T>A	XP_006721371.1:p.Thr242=
XM_006721310.1:c.726T>A	XP_006721373.1:p.Thr242=
XM_011523405.1:c.822T>A	XP_011521707.1:p.Thr274=
XM_011523406.1:c.822T>A	XP_011521708.1:p.Thr274=
XM_011523407.1:c.822T>A	XP_011521709.1:p.Thr274=
XM_011523408.1:c.822T>A	XP_011521710.1:p.Thr274=
XM_011523409.1:c.711T>A	XP_011521711.1:p.Thr237=
XM_011523410.1:c.609T>A	XP_011521712.1:p.Thr203=
XM_011523411.1:c.609T>A	XP_011521713.1:p.Thr203=
XM_011523412.1:c.609T>A	XP_011521714.1:p.Thr203=
XM_011523413.1:c.609T>A	XP_011521715.1:p.Thr203=
XM_011523414.1:c.609T>A	XP_011521716.1:p.Thr203=
XM_011523415.1:c.609T>A	XP_011521717.1:p.Thr203=
XM_011523416.1:c.609T>A	XP_011521718.1:p.Thr203=
XR_933471.1:n.2743T>A
XM_006721308.3:c.726T>A	XP_006721371.1:p.Thr242=
XM_006721310.3:c.726T>A	XP_006721373.1:p.Thr242=
XM_011523405.3:c.822T>A	XP_011521707.1:p.Thr274=
XM_011523406.3:c.822T>A	XP_011521708.1:p.Thr274=
XM_011523407.3:c.822T>A	XP_011521709.1:p.Thr274=
XM_011523408.3:c.822T>A	XP_011521710.1:p.Thr274=
XM_011523410.2:c.609T>A	XP_011521712.1:p.Thr203=
XM_011523411.2:c.609T>A	XP_011521713.1:p.Thr203=
XM_011523413.2:c.609T>A	XP_011521715.1:p.Thr203=
XM_011523414.2:c.609T>A	XP_011521716.1:p.Thr203=
XM_011523415.3:c.609T>A	XP_011521717.1:p.Thr203=
XM_011523416.2:c.609T>A	XP_011521718.1:p.Thr203=
XM_017023806.1:c.711T>A	XP_016879295.1:p.Thr237=
XM_017023807.2:c.726T>A	XP_016879296.1:p.Thr242=
XM_017023808.1:c.513T>A	XP_016879297.1:p.Thr171=
XM_017023809.2:c.513T>A	XP_016879298.1:p.Thr171=
XM_017023810.1:c.513T>A	XP_016879299.1:p.Thr171=
NM_052988.5:c.726T>A MANE Select	NP_443714.3:p.Thr242=
NM_001098533.3:c.513T>A	NP_001092003.2:p.Thr171=
NM_001160367.2:c.513T>A	NP_001153839.1:p.Thr171=
NM_052987.4:c.513T>A	NP_443713.2:p.Thr171=
NR_027702.2:n.675T>A
NR_027703.2:n.675T>A