Canonical Allele Identifier: CA1701738290
Gene: CDK13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.39999518_39999519delinsTG , CM000669.2:g.39999518_39999519delinsTG GRCh38
NC_000007.13:g.40039117_40039118delinsTG , CM000669.1:g.40039117_40039118delinsTG GRCh37
NC_000007.12:g.40005642_40005643delinsTG NCBI36
NG_052965.1:g.54159_54160delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000181839.10:c.2182+18_2182+19delinsTG MANE Select ENSP00000181839.4:n.2182+18_2182+19delinsTG
ENST00000340829.10:c.2182+18_2182+19delinsTG ENSP00000340557.5:n.2182+18_2182+19delinsTG
ENST00000484589.2:c.734+18_734+19delinsTG
ENST00000642213.1:n.664+18_664+19delinsTG
ENST00000643859.1:c.1073+18_1073+19delinsTG
ENST00000643915.1:c.496+18_496+19delinsTG ENSP00000496187.1:n.496+18_496+19delinsTG
ENST00000645470.1:c.112+18_112+19delinsTG ENSP00000495036.1:n.112+18_112+19delinsTG
ENST00000646039.1:c.1522+18_1522+19delinsTG ENSP00000494168.1:n.1522+18_1522+19delinsTG
ENST00000647453.1:n.1251+18_1251+19delinsTG
ENST00000647518.1:n.4019+18_4019+19delinsTG
ENST00000181839.8:c.2182+18_2182+19delinsTG ENSP00000181839.4:n.2182+18_2182+19delinsTG
ENST00000340829.9:c.2182+18_2182+19delinsTG ENSP00000340557.5:n.2182+18_2182+19delinsTG
ENST00000484589.1:n.734+18_734+19delinsTG
ENST00000611390.1:c.340+18_340+19delinsTG ENSP00000484610.1:n.340+18_340+19delinsTG
ENST00000613626.4:c.340+18_340+19delinsTG ENSP00000480835.1:n.340+18_340+19delinsTG
NM_003718.4:c.2182+18_2182+19delinsTG NP_003709.3:n.2182+18_2182+19delinsTG
NM_031267.3:c.2182+18_2182+19delinsTG NP_112557.2:n.2182+18_2182+19delinsTG
XM_011515597.1:c.2182+18_2182+19delinsTG XP_011513899.1:n.2182+18_2182+19delinsTG
XM_011515598.1:c.2182+18_2182+19delinsTG XP_011513900.1:n.2182+18_2182+19delinsTG
XM_011515597.3:c.2182+18_2182+19delinsTG XP_011513899.1:n.2182+18_2182+19delinsTG
XM_017012750.2:c.2182+18_2182+19delinsTG XP_016868239.1:n.2182+18_2182+19delinsTG
XM_017012751.2:c.2182+18_2182+19delinsTG XP_016868240.1:n.2182+18_2182+19delinsTG
NM_003718.5:c.2182+18_2182+19delinsTG MANE Select NP_003709.3:n.2182+18_2182+19delinsTG