Canonical Allele Identifier: CA14322145

Gene: CDK10

Linked Data

• dbSNP Id: rs258322
• gnomAD v2: 16-89755903-A-G
• gnomAD v3: 16-89689495-A-G
• gnomAD v4: 16-89689495-A-G
• MyVariant Identifiers: chr16:g.89755903A>G (hg19) ; chr16:g.89689495A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89689495A>G , CM000678.2:g.89689495A>G	GRCh38
NC_000016.9:g.89755903A>G , CM000678.1:g.89755903A>G	GRCh37
NC_000016.8:g.88283404A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000353379.12:c.160+171A>G MANE Select	ENSP00000338673.7:n.160+171A>G
ENST00000331006.12:c.20-1058A>G	ENSP00000329957.8:n.20-1058A>G
ENST00000353379.11:c.160+171A>G	ENSP00000338673.7:n.160+171A>G
ENST00000378277.8:n.86-1058A>G
ENST00000472018.5:n.171+171A>G
ENST00000502547.5:c.*177+171A>G	ENSP00000421597.1:n.*177+171A>G
ENST00000503560.1:n.457+171A>G
ENST00000504473.5:n.364-1058A>G
ENST00000505473.5:c.-54+171A>G	ENSP00000424415.1:n.-54+171A>G
ENST00000505733.5:n.181+171A>G
ENST00000507205.5:n.123+189A>G
ENST00000508723.5:c.*220+171A>G	ENSP00000423370.1:n.*220+171A>G
ENST00000510811.6:c.88-1058A>G	ENSP00000455976.1:n.88-1058A>G
ENST00000511415.5:c.*51+171A>G	ENSP00000426102.1:n.*51+171A>G
ENST00000512912.5:c.*105-1058A>G	ENSP00000426264.1:n.*105-1058A>G
ENST00000514965.5:n.332+171A>G
ENST00000564192.5:c.-54+171A>G	ENSP00000457055.1:n.-54+171A>G
ENST00000625631.1:c.88-1058A>G	ENSP00000486594.1:n.88-1058A>G
NM_001098533.2:c.-54+171A>G	NP_001092003.2:n.-54+171A>G
NM_001160367.1:c.-54+171A>G	NP_001153839.1:n.-54+171A>G
NM_052987.3:c.-54+171A>G	NP_443713.2:n.-54+171A>G
NM_052988.4:c.160+171A>G	NP_443714.3:n.160+171A>G
NR_027702.1:n.131-1058A>G
NR_027703.1:n.131-1058A>G
XM_006721308.1:c.160+171A>G	XP_006721371.1:n.160+171A>G
XM_006721310.1:c.160+171A>G	XP_006721373.1:n.160+171A>G
XM_011523405.1:c.160+171A>G	XP_011521707.1:n.160+171A>G
XM_011523406.1:c.160+171A>G	XP_011521708.1:n.160+171A>G
XM_011523407.1:c.160+171A>G	XP_011521709.1:n.160+171A>G
XM_011523408.1:c.160+171A>G	XP_011521710.1:n.160+171A>G
XM_011523409.1:c.50-1058A>G	XP_011521711.1:n.50-1058A>G
XM_011523410.1:c.-54+171A>G	XP_011521712.1:n.-54+171A>G
XM_011523411.1:c.-54+171A>G	XP_011521713.1:n.-54+171A>G
XM_011523412.1:c.-54+171A>G	XP_011521714.1:n.-54+171A>G
XM_011523413.1:c.-54+171A>G	XP_011521715.1:n.-54+171A>G
XM_011523414.1:c.-54+171A>G	XP_011521716.1:n.-54+171A>G
XM_011523415.1:c.-53-1058A>G	XP_011521717.1:n.-53-1058A>G
XM_011523416.1:c.-53-1058A>G	XP_011521718.1:n.-53-1058A>G
XM_011523417.1:c.160+171A>G	XP_011521719.1:n.160+171A>G
XM_011523418.1:c.160+171A>G	XP_011521720.1:n.160+171A>G
XR_933471.1:n.2106+171A>G
XM_006721308.3:c.160+171A>G	XP_006721371.1:n.160+171A>G
XM_006721310.3:c.160+171A>G	XP_006721373.1:n.160+171A>G
XM_011523405.3:c.160+171A>G	XP_011521707.1:n.160+171A>G
XM_011523406.3:c.160+171A>G	XP_011521708.1:n.160+171A>G
XM_011523407.3:c.160+171A>G	XP_011521709.1:n.160+171A>G
XM_011523408.3:c.160+171A>G	XP_011521710.1:n.160+171A>G
XM_011523410.2:c.-54+171A>G	XP_011521712.1:n.-54+171A>G
XM_011523411.2:c.-54+171A>G	XP_011521713.1:n.-54+171A>G
XM_011523413.2:c.-54+171A>G	XP_011521715.1:n.-54+171A>G
XM_011523414.2:c.-54+171A>G	XP_011521716.1:n.-54+171A>G
XM_011523415.3:c.-53-1058A>G	XP_011521717.1:n.-53-1058A>G
XM_011523416.2:c.-53-1058A>G	XP_011521718.1:n.-53-1058A>G
XM_011523417.3:c.160+171A>G	XP_011521719.1:n.160+171A>G
XM_017023806.1:c.50-1058A>G	XP_016879295.1:n.50-1058A>G
XM_017023807.2:c.160+171A>G	XP_016879296.1:n.160+171A>G
XM_017023808.1:c.-54+171A>G	XP_016879297.1:n.-54+171A>G
XM_017023809.2:c.-53-1058A>G	XP_016879298.1:n.-53-1058A>G
XM_017023810.1:c.-54+171A>G	XP_016879299.1:n.-54+171A>G
NM_052988.5:c.160+171A>G MANE Select	NP_443714.3:n.160+171A>G
NM_001098533.3:c.-54+171A>G	NP_001092003.2:n.-54+171A>G
NM_001160367.2:c.-54+171A>G	NP_001153839.1:n.-54+171A>G
NM_052987.4:c.-54+171A>G	NP_443713.2:n.-54+171A>G
NR_027702.2:n.110-1058A>G
NR_027703.2:n.110-1058A>G