Canonical Allele Identifier: CA233652

Gene: CDK16

Linked Data

• ClinVar Variation Id: 166819
• ClinVar RCV Id: RCV000152957
• dbSNP Id: rs727503845
• MyVariant Identifiers: chrX:g.47086497C>T (hg19) ; chrX:g.47227098C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47227098C>T , CM000685.2:g.47227098C>T	GRCh38
NC_000023.10:g.47086497C>T , CM000685.1:g.47086497C>T	GRCh37
NC_000023.9:g.46971441C>T	NCBI36
NG_012517.1:g.13970C>T
NG_012517.2:g.13970C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357227.9:c.1240C>T MANE Select	ENSP00000349762.4:p.Arg414Ter
ENST00000276052.10:c.1462C>T	ENSP00000276052.6:p.Arg488Ter
ENST00000357227.8:c.1240C>T	ENSP00000349762.4:p.Arg414Ter
ENST00000428400.5:n.2376C>T
ENST00000457458.6:c.1258C>T	ENSP00000405798.2:p.Arg420Ter
ENST00000517426.5:c.1135+189C>T	ENSP00000429985.1:n.1135+189C>T
ENST00000518022.5:c.1240C>T	ENSP00000429751.1:p.Arg414Ter
ENST00000523344.5:c.511C>T	ENSP00000428349.1:p.Arg171Trp
ENST00000523543.1:n.415C>T
ENST00000523699.5:n.631C>T
ENST00000622098.4:c.1096C>T	ENSP00000482886.1:p.Arg366Ter
NM_001170460.1:c.1462C>T	NP_001163931.1:p.Arg488Ter
NM_006201.4:c.1240C>T	NP_006192.1:p.Arg414Ter
NM_033018.3:c.1258C>T	NP_148978.2:p.Arg420Ter
XM_011543920.1:c.1462C>T	XP_011542222.1:p.Arg488Ter
XM_011543921.1:c.1381C>T	XP_011542223.1:p.Arg461Ter
XM_011543922.1:c.1369C>T	XP_011542224.1:p.Arg457Ter
XM_011543923.1:c.1258C>T	XP_011542225.1:p.Arg420Ter
XM_011543924.1:c.1240C>T	XP_011542226.1:p.Arg414Ter
XM_011543925.1:c.1240C>T	XP_011542227.1:p.Arg414Ter
XM_011543926.1:c.1240C>T	XP_011542228.1:p.Arg414Ter
XM_011543927.1:c.1240C>T	XP_011542229.1:p.Arg414Ter
XM_011543928.1:c.1240C>T	XP_011542230.1:p.Arg414Ter
XR_949017.1:n.1420C>T
XM_011543920.3:c.1462C>T	XP_011542222.1:p.Arg488Ter
XM_011543923.2:c.1258C>T	XP_011542225.1:p.Arg420Ter
XM_011543924.2:c.1240C>T	XP_011542226.1:p.Arg414Ter
XM_011543925.3:c.1240C>T	XP_011542227.1:p.Arg414Ter
XM_011543927.3:c.1240C>T	XP_011542229.1:p.Arg414Ter
XM_017029569.1:c.1381C>T	XP_016885058.1:p.Arg461Ter
XM_017029570.2:c.1240C>T	XP_016885059.1:p.Arg414Ter
XM_017029571.1:c.1240C>T	XP_016885060.1:p.Arg414Ter
XM_017029572.2:c.1240C>T	XP_016885061.1:p.Arg414Ter
XM_017029573.1:c.1240C>T	XP_016885062.1:p.Arg414Ter
XR_949017.3:n.1443C>T
NM_006201.5:c.1240C>T MANE Select	NP_006192.1:p.Arg414Ter
NM_033018.4:c.1258C>T	NP_148978.2:p.Arg420Ter
NM_001170460.2:c.1462C>T	NP_001163931.1:p.Arg488Ter