Canonical Allele Identifier: CA1701738407

Gene: CDK13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999752_39999756delinsTTTTC , CM000669.2:g.39999752_39999756delinsTTTTC	GRCh38
NC_000007.13:g.40039351_40039355delinsTTTTC , CM000669.1:g.40039351_40039355delinsTTTTC	GRCh37
NC_000007.12:g.40005876_40005880delinsTTTTC	NCBI36
NG_052965.1:g.54393_54397delinsTTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2182+252_2182+256delinsTTTTC MANE Select	ENSP00000181839.4:n.2182+252_2182+256delinsTTTTC
ENST00000340829.10:c.2182+252_2182+256delinsTTTTC	ENSP00000340557.5:n.2182+252_2182+256delinsTTTTC
ENST00000484589.2:c.734+252_734+256delinsTTTTC
ENST00000642213.1:n.664+252_664+256delinsTTTTC
ENST00000643859.1:c.1073+252_1073+256delinsTTTTC
ENST00000643915.1:c.496+252_496+256delinsTTTTC	ENSP00000496187.1:n.496+252_496+256delinsTTTTC
ENST00000645470.1:c.112+252_112+256delinsTTTTC	ENSP00000495036.1:n.112+252_112+256delinsTTTTC
ENST00000646039.1:c.1522+252_1522+256delinsTTTTC	ENSP00000494168.1:n.1522+252_1522+256delinsTTTTC
ENST00000647453.1:n.1251+252_1251+256delinsTTTTC
ENST00000647518.1:n.4019+252_4019+256delinsTTTTC
ENST00000181839.8:c.2182+252_2182+256delinsTTTTC	ENSP00000181839.4:n.2182+252_2182+256delinsTTTTC
ENST00000340829.9:c.2182+252_2182+256delinsTTTTC	ENSP00000340557.5:n.2182+252_2182+256delinsTTTTC
ENST00000484589.1:n.734+252_734+256delinsTTTTC
ENST00000611390.1:c.340+252_340+256delinsTTTTC	ENSP00000484610.1:n.340+252_340+256delinsTTTTC
ENST00000613626.4:c.340+252_340+256delinsTTTTC	ENSP00000480835.1:n.340+252_340+256delinsTTTTC
NM_003718.4:c.2182+252_2182+256delinsTTTTC	NP_003709.3:n.2182+252_2182+256delinsTTTTC
NM_031267.3:c.2182+252_2182+256delinsTTTTC	NP_112557.2:n.2182+252_2182+256delinsTTTTC
XM_011515597.1:c.2182+252_2182+256delinsTTTTC	XP_011513899.1:n.2182+252_2182+256delinsTTTTC
XM_011515598.1:c.2182+252_2182+256delinsTTTTC	XP_011513900.1:n.2182+252_2182+256delinsTTTTC
XM_011515597.3:c.2182+252_2182+256delinsTTTTC	XP_011513899.1:n.2182+252_2182+256delinsTTTTC
XM_017012750.2:c.2182+252_2182+256delinsTTTTC	XP_016868239.1:n.2182+252_2182+256delinsTTTTC
XM_017012751.2:c.2182+252_2182+256delinsTTTTC	XP_016868240.1:n.2182+252_2182+256delinsTTTTC
NM_003718.5:c.2182+252_2182+256delinsTTTTC MANE Select	NP_003709.3:n.2182+252_2182+256delinsTTTTC