Canonical Allele Identifier: CA367288016
Gene: CDK13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.39999390A>C , CM000669.2:g.39999390A>C GRCh38
NC_000007.13:g.40038989A>C , CM000669.1:g.40038989A>C GRCh37
NC_000007.12:g.40005514A>C NCBI36
NG_052965.1:g.54031A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000181839.10:c.2072A>C MANE Select ENSP00000181839.4:p.Lys691Thr
ENST00000340829.10:c.2072A>C ENSP00000340557.5:p.Lys691Thr
ENST00000484589.2:c.624A>C
ENST00000642213.1:n.554A>C
ENST00000643859.1:c.963A>C
ENST00000643915.1:c.386A>C ENSP00000496187.1:p.Lys129Thr
ENST00000645470.1:c.2A>C ENSP00000495036.1:p.Lys1Thr
ENST00000646039.1:c.1412A>C ENSP00000494168.1:p.Lys471Thr
ENST00000646437.1:c.706A>C
ENST00000647453.1:n.1141A>C
ENST00000647518.1:n.3909A>C
ENST00000181839.8:c.2072A>C ENSP00000181839.4:p.Lys691Thr
ENST00000340829.9:c.2072A>C ENSP00000340557.5:p.Lys691Thr
ENST00000484589.1:n.624A>C
ENST00000611390.1:c.230A>C ENSP00000484610.1:p.Lys77Thr
ENST00000613626.4:c.230A>C ENSP00000480835.1:p.Lys77Thr
NM_003718.4:c.2072A>C NP_003709.3:p.Lys691Thr
NM_031267.3:c.2072A>C NP_112557.2:p.Lys691Thr
XM_011515597.1:c.2072A>C XP_011513899.1:p.Lys691Thr
XM_011515598.1:c.2072A>C XP_011513900.1:p.Lys691Thr
XM_011515597.3:c.2072A>C XP_011513899.1:p.Lys691Thr
XM_017012750.2:c.2072A>C XP_016868239.1:p.Lys691Thr
XM_017012751.2:c.2072A>C XP_016868240.1:p.Lys691Thr
NM_003718.5:c.2072A>C MANE Select NP_003709.3:p.Lys691Thr