Canonical Allele Identifier: CA397424316

Gene: CDK10

Linked Data

• MyVariant Identifiers: chr16:g.89761137A>G (hg19) ; chr16:g.89694729A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89694729A>G , CM000678.2:g.89694729A>G	GRCh38
NC_000016.9:g.89761137A>G , CM000678.1:g.89761137A>G	GRCh37
NC_000016.8:g.88288638A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000353379.12:c.733A>G MANE Select	ENSP00000338673.7:p.Ile245Val
ENST00000331006.12:c.592A>G	ENSP00000329957.8:p.Ile198Val
ENST00000353379.11:c.733A>G	ENSP00000338673.7:p.Ile245Val
ENST00000472018.5:n.1520A>G
ENST00000505473.5:c.520A>G	ENSP00000424415.1:p.Ile174Val
ENST00000505733.5:n.825A>G
ENST00000510811.6:c.*531A>G	ENSP00000455976.1:n.*531A>G
ENST00000564192.5:c.616A>G	ENSP00000457055.1:p.Ile206Val
ENST00000565470.1:c.50-202A>G
ENST00000617879.1:c.520A>G	ENSP00000484357.1:p.Ile174Val
NM_001098533.2:c.520A>G	NP_001092003.2:p.Ile174Val
NM_001160367.1:c.520A>G	NP_001153839.1:p.Ile174Val
NM_052987.3:c.520A>G	NP_443713.2:p.Ile174Val
NM_052988.4:c.733A>G	NP_443714.3:p.Ile245Val
NR_027702.1:n.703A>G
NR_027703.1:n.703A>G
XM_006721308.1:c.733A>G	XP_006721371.1:p.Ile245Val
XM_006721310.1:c.733A>G	XP_006721373.1:p.Ile245Val
XM_011523405.1:c.829A>G	XP_011521707.1:p.Ile277Val
XM_011523406.1:c.829A>G	XP_011521708.1:p.Ile277Val
XM_011523407.1:c.829A>G	XP_011521709.1:p.Ile277Val
XM_011523408.1:c.829A>G	XP_011521710.1:p.Ile277Val
XM_011523409.1:c.718A>G	XP_011521711.1:p.Ile240Val
XM_011523410.1:c.616A>G	XP_011521712.1:p.Ile206Val
XM_011523411.1:c.616A>G	XP_011521713.1:p.Ile206Val
XM_011523412.1:c.616A>G	XP_011521714.1:p.Ile206Val
XM_011523413.1:c.616A>G	XP_011521715.1:p.Ile206Val
XM_011523414.1:c.616A>G	XP_011521716.1:p.Ile206Val
XM_011523415.1:c.616A>G	XP_011521717.1:p.Ile206Val
XM_011523416.1:c.616A>G	XP_011521718.1:p.Ile206Val
XR_933471.1:n.2750A>G
XM_006721308.3:c.733A>G	XP_006721371.1:p.Ile245Val
XM_006721310.3:c.733A>G	XP_006721373.1:p.Ile245Val
XM_011523405.3:c.829A>G	XP_011521707.1:p.Ile277Val
XM_011523406.3:c.829A>G	XP_011521708.1:p.Ile277Val
XM_011523407.3:c.829A>G	XP_011521709.1:p.Ile277Val
XM_011523408.3:c.829A>G	XP_011521710.1:p.Ile277Val
XM_011523410.2:c.616A>G	XP_011521712.1:p.Ile206Val
XM_011523411.2:c.616A>G	XP_011521713.1:p.Ile206Val
XM_011523413.2:c.616A>G	XP_011521715.1:p.Ile206Val
XM_011523414.2:c.616A>G	XP_011521716.1:p.Ile206Val
XM_011523415.3:c.616A>G	XP_011521717.1:p.Ile206Val
XM_011523416.2:c.616A>G	XP_011521718.1:p.Ile206Val
XM_017023806.1:c.718A>G	XP_016879295.1:p.Ile240Val
XM_017023807.2:c.733A>G	XP_016879296.1:p.Ile245Val
XM_017023808.1:c.520A>G	XP_016879297.1:p.Ile174Val
XM_017023809.2:c.520A>G	XP_016879298.1:p.Ile174Val
XM_017023810.1:c.520A>G	XP_016879299.1:p.Ile174Val
NM_052988.5:c.733A>G MANE Select	NP_443714.3:p.Ile245Val
NM_001098533.3:c.520A>G	NP_001092003.2:p.Ile174Val
NM_001160367.2:c.520A>G	NP_001153839.1:p.Ile174Val
NM_052987.4:c.520A>G	NP_443713.2:p.Ile174Val
NR_027702.2:n.682A>G
NR_027703.2:n.682A>G