Canonical Allele Identifier: CA1701738344

Gene: CDK13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999628_39999630delinsCTT , CM000669.2:g.39999628_39999630delinsCTT	GRCh38
NC_000007.13:g.40039227_40039229delinsCTT , CM000669.1:g.40039227_40039229delinsCTT	GRCh37
NC_000007.12:g.40005752_40005754delinsCTT	NCBI36
NG_052965.1:g.54269_54271delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2182+128_2182+130delinsCTT MANE Select	ENSP00000181839.4:n.2182+128_2182+130delinsCTT
ENST00000340829.10:c.2182+128_2182+130delinsCTT	ENSP00000340557.5:n.2182+128_2182+130delinsCTT
ENST00000484589.2:c.734+128_734+130delinsCTT
ENST00000642213.1:n.664+128_664+130delinsCTT
ENST00000643859.1:c.1073+128_1073+130delinsCTT
ENST00000643915.1:c.496+128_496+130delinsCTT	ENSP00000496187.1:n.496+128_496+130delinsCTT
ENST00000645470.1:c.112+128_112+130delinsCTT	ENSP00000495036.1:n.112+128_112+130delinsCTT
ENST00000646039.1:c.1522+128_1522+130delinsCTT	ENSP00000494168.1:n.1522+128_1522+130delinsCTT
ENST00000647453.1:n.1251+128_1251+130delinsCTT
ENST00000647518.1:n.4019+128_4019+130delinsCTT
ENST00000181839.8:c.2182+128_2182+130delinsCTT	ENSP00000181839.4:n.2182+128_2182+130delinsCTT
ENST00000340829.9:c.2182+128_2182+130delinsCTT	ENSP00000340557.5:n.2182+128_2182+130delinsCTT
ENST00000484589.1:n.734+128_734+130delinsCTT
ENST00000611390.1:c.340+128_340+130delinsCTT	ENSP00000484610.1:n.340+128_340+130delinsCTT
ENST00000613626.4:c.340+128_340+130delinsCTT	ENSP00000480835.1:n.340+128_340+130delinsCTT
NM_003718.4:c.2182+128_2182+130delinsCTT	NP_003709.3:n.2182+128_2182+130delinsCTT
NM_031267.3:c.2182+128_2182+130delinsCTT	NP_112557.2:n.2182+128_2182+130delinsCTT
XM_011515597.1:c.2182+128_2182+130delinsCTT	XP_011513899.1:n.2182+128_2182+130delinsCTT
XM_011515598.1:c.2182+128_2182+130delinsCTT	XP_011513900.1:n.2182+128_2182+130delinsCTT
XM_011515597.3:c.2182+128_2182+130delinsCTT	XP_011513899.1:n.2182+128_2182+130delinsCTT
XM_017012750.2:c.2182+128_2182+130delinsCTT	XP_016868239.1:n.2182+128_2182+130delinsCTT
XM_017012751.2:c.2182+128_2182+130delinsCTT	XP_016868240.1:n.2182+128_2182+130delinsCTT
NM_003718.5:c.2182+128_2182+130delinsCTT MANE Select	NP_003709.3:n.2182+128_2182+130delinsCTT