Canonical Allele Identifier: CA1701738272
Gene: CDK13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.39999476T= , CM000669.2:g.39999476T= GRCh38
NC_000007.13:g.40039075T= , CM000669.1:g.40039075T= GRCh37
NC_000007.12:g.40005600T= NCBI36
NG_052965.1:g.54117T=

Transcript Alleles

HGVS Amino-acid change
ENST00000181839.10:c.2158T= MANE Select ENSP00000181839.4:p.Tyr720=
ENST00000340829.10:c.2158T= ENSP00000340557.5:p.Tyr720=
ENST00000484589.2:c.710T=
ENST00000642213.1:n.640T=
ENST00000643859.1:c.1049T=
ENST00000643915.1:c.472T= ENSP00000496187.1:p.Tyr158=
ENST00000645470.1:c.88T= ENSP00000495036.1:p.Tyr30=
ENST00000646039.1:c.1498T= ENSP00000494168.1:p.Tyr500=
ENST00000647453.1:n.1227T=
ENST00000647518.1:n.3995T=
ENST00000181839.8:c.2158T= ENSP00000181839.4:p.Tyr720=
ENST00000340829.9:c.2158T= ENSP00000340557.5:p.Tyr720=
ENST00000484589.1:n.710T=
ENST00000611390.1:c.316T= ENSP00000484610.1:p.Tyr106=
ENST00000613626.4:c.316T= ENSP00000480835.1:p.Tyr106=
NM_003718.4:c.2158T= NP_003709.3:p.Tyr720=
NM_031267.3:c.2158T= NP_112557.2:p.Tyr720=
XM_011515597.1:c.2158T= XP_011513899.1:p.Tyr720=
XM_011515598.1:c.2158T= XP_011513900.1:p.Tyr720=
XM_011515597.3:c.2158T= XP_011513899.1:p.Tyr720=
XM_017012750.2:c.2158T= XP_016868239.1:p.Tyr720=
XM_017012751.2:c.2158T= XP_016868240.1:p.Tyr720=
NM_003718.5:c.2158T= MANE Select NP_003709.3:p.Tyr720=