Canonical Allele Identifier: CA838356258
Gene: CDK13 HGNC NCBI

Linked Data

dbSNP Id: rs1225165679

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.39999305_39999308del , CM000669.2:g.39999305_39999308del GRCh38
NC_000007.13:g.40038904_40038907del , CM000669.1:g.40038904_40038907del GRCh37
NC_000007.12:g.40005429_40005432del NCBI36
NG_052965.1:g.53946_53949del

Transcript Alleles

HGVS Amino-acid Change
ENST00000181839.10:c.2043-56_2043-53del MANE Select ENSP00000181839.4:n.2043-56_2043-53del
ENST00000340829.10:c.2043-56_2043-53del ENSP00000340557.5:n.2043-56_2043-53del
ENST00000484589.2:c.595-56_595-53del
ENST00000642213.1:n.469_472del
ENST00000642660.1:n.923-56_923-53del
ENST00000643859.1:c.934-56_934-53del
ENST00000643915.1:c.357-56_357-53del ENSP00000496187.1:n.357-56_357-53del
ENST00000646039.1:c.1383-56_1383-53del ENSP00000494168.1:n.1383-56_1383-53del
ENST00000646437.1:c.662-41_662-38del
ENST00000647453.1:n.1056_1059del
ENST00000647518.1:n.3880-56_3880-53del
ENST00000181839.8:c.2043-56_2043-53del ENSP00000181839.4:n.2043-56_2043-53del
ENST00000340829.9:c.2043-56_2043-53del ENSP00000340557.5:n.2043-56_2043-53del
ENST00000484589.1:n.595-56_595-53del
ENST00000611390.1:c.201-56_201-53del ENSP00000484610.1:n.201-56_201-53del
ENST00000613626.4:c.201-56_201-53del ENSP00000480835.1:n.201-56_201-53del
NM_003718.4:c.2043-56_2043-53del NP_003709.3:n.2043-56_2043-53del
NM_031267.3:c.2043-56_2043-53del NP_112557.2:n.2043-56_2043-53del
XM_011515597.1:c.2043-56_2043-53del XP_011513899.1:n.2043-56_2043-53del
XM_011515598.1:c.2043-56_2043-53del XP_011513900.1:n.2043-56_2043-53del
XM_011515597.3:c.2043-56_2043-53del XP_011513899.1:n.2043-56_2043-53del
XM_017012750.2:c.2043-56_2043-53del XP_016868239.1:n.2043-56_2043-53del
XM_017012751.2:c.2043-56_2043-53del XP_016868240.1:n.2043-56_2043-53del
NM_003718.5:c.2043-56_2043-53del MANE Select NP_003709.3:n.2043-56_2043-53del