Canonical Allele Identifier: CA367287957
Gene: CDK13 HGNC NCBI

Linked Data

COSMIC: COSM453032

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.39999363T>A , CM000669.2:g.39999363T>A GRCh38
NC_000007.13:g.40038962T>A , CM000669.1:g.40038962T>A GRCh37
NC_000007.12:g.40005487T>A NCBI36
NG_052965.1:g.54004T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000181839.10:c.2045T>A MANE Select ENSP00000181839.4:p.Ile682Lys
ENST00000340829.10:c.2045T>A ENSP00000340557.5:p.Ile682Lys
ENST00000484589.2:c.597T>A
ENST00000642213.1:n.527T>A
ENST00000642660.1:n.925T>A
ENST00000643859.1:c.936T>A
ENST00000643915.1:c.359T>A ENSP00000496187.1:p.Ile120Lys
ENST00000646039.1:c.1385T>A ENSP00000494168.1:p.Ile462Lys
ENST00000646437.1:c.679T>A
ENST00000647453.1:n.1114T>A
ENST00000647518.1:n.3882T>A
ENST00000181839.8:c.2045T>A ENSP00000181839.4:p.Ile682Lys
ENST00000340829.9:c.2045T>A ENSP00000340557.5:p.Ile682Lys
ENST00000484589.1:n.597T>A
ENST00000611390.1:c.203T>A ENSP00000484610.1:p.Ile68Lys
ENST00000613626.4:c.203T>A ENSP00000480835.1:p.Ile68Lys
NM_003718.4:c.2045T>A NP_003709.3:p.Ile682Lys
NM_031267.3:c.2045T>A NP_112557.2:p.Ile682Lys
XM_011515597.1:c.2045T>A XP_011513899.1:p.Ile682Lys
XM_011515598.1:c.2045T>A XP_011513900.1:p.Ile682Lys
XM_011515597.3:c.2045T>A XP_011513899.1:p.Ile682Lys
XM_017012750.2:c.2045T>A XP_016868239.1:p.Ile682Lys
XM_017012751.2:c.2045T>A XP_016868240.1:p.Ile682Lys
NM_003718.5:c.2045T>A MANE Select NP_003709.3:p.Ile682Lys