Canonical Allele Identifier: CA497377651

Gene: CDK10

Linked Data

• dbSNP Id: rs2060622717
• MyVariant Identifiers: chr16:g.89761139C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89694731C>T , CM000678.2:g.89694731C>T	GRCh38
NC_000016.9:g.89761139C>T , CM000678.1:g.89761139C>T	GRCh37
NC_000016.8:g.88288640C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000353379.12:c.735C>T MANE Select	ENSP00000338673.7:p.Ile245=
ENST00000331006.12:c.594C>T	ENSP00000329957.8:p.Ile198=
ENST00000353379.11:c.735C>T	ENSP00000338673.7:p.Ile245=
ENST00000472018.5:n.1522C>T
ENST00000505473.5:c.522C>T	ENSP00000424415.1:p.Ile174=
ENST00000505733.5:n.827C>T
ENST00000510811.6:c.*533C>T	ENSP00000455976.1:n.*533C>T
ENST00000564192.5:c.618C>T	ENSP00000457055.1:p.Ile206=
ENST00000565470.1:c.50-200C>T
ENST00000617879.1:c.522C>T	ENSP00000484357.1:p.Ile174=
NM_001098533.2:c.522C>T	NP_001092003.2:p.Ile174=
NM_001160367.1:c.522C>T	NP_001153839.1:p.Ile174=
NM_052987.3:c.522C>T	NP_443713.2:p.Ile174=
NM_052988.4:c.735C>T	NP_443714.3:p.Ile245=
NR_027702.1:n.705C>T
NR_027703.1:n.705C>T
XM_006721308.1:c.735C>T	XP_006721371.1:p.Ile245=
XM_006721310.1:c.735C>T	XP_006721373.1:p.Ile245=
XM_011523405.1:c.831C>T	XP_011521707.1:p.Ile277=
XM_011523406.1:c.831C>T	XP_011521708.1:p.Ile277=
XM_011523407.1:c.831C>T	XP_011521709.1:p.Ile277=
XM_011523408.1:c.831C>T	XP_011521710.1:p.Ile277=
XM_011523409.1:c.720C>T	XP_011521711.1:p.Ile240=
XM_011523410.1:c.618C>T	XP_011521712.1:p.Ile206=
XM_011523411.1:c.618C>T	XP_011521713.1:p.Ile206=
XM_011523412.1:c.618C>T	XP_011521714.1:p.Ile206=
XM_011523413.1:c.618C>T	XP_011521715.1:p.Ile206=
XM_011523414.1:c.618C>T	XP_011521716.1:p.Ile206=
XM_011523415.1:c.618C>T	XP_011521717.1:p.Ile206=
XM_011523416.1:c.618C>T	XP_011521718.1:p.Ile206=
XR_933471.1:n.2752C>T
XM_006721308.3:c.735C>T	XP_006721371.1:p.Ile245=
XM_006721310.3:c.735C>T	XP_006721373.1:p.Ile245=
XM_011523405.3:c.831C>T	XP_011521707.1:p.Ile277=
XM_011523406.3:c.831C>T	XP_011521708.1:p.Ile277=
XM_011523407.3:c.831C>T	XP_011521709.1:p.Ile277=
XM_011523408.3:c.831C>T	XP_011521710.1:p.Ile277=
XM_011523410.2:c.618C>T	XP_011521712.1:p.Ile206=
XM_011523411.2:c.618C>T	XP_011521713.1:p.Ile206=
XM_011523413.2:c.618C>T	XP_011521715.1:p.Ile206=
XM_011523414.2:c.618C>T	XP_011521716.1:p.Ile206=
XM_011523415.3:c.618C>T	XP_011521717.1:p.Ile206=
XM_011523416.2:c.618C>T	XP_011521718.1:p.Ile206=
XM_017023806.1:c.720C>T	XP_016879295.1:p.Ile240=
XM_017023807.2:c.735C>T	XP_016879296.1:p.Ile245=
XM_017023808.1:c.522C>T	XP_016879297.1:p.Ile174=
XM_017023809.2:c.522C>T	XP_016879298.1:p.Ile174=
XM_017023810.1:c.522C>T	XP_016879299.1:p.Ile174=
NM_052988.5:c.735C>T MANE Select	NP_443714.3:p.Ile245=
NM_001098533.3:c.522C>T	NP_001092003.2:p.Ile174=
NM_001160367.2:c.522C>T	NP_001153839.1:p.Ile174=
NM_052987.4:c.522C>T	NP_443713.2:p.Ile174=
NR_027702.2:n.684C>T
NR_027703.2:n.684C>T