Canonical Allele Identifier: CA367288183
Gene: CDK13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.39999429A>C , CM000669.2:g.39999429A>C GRCh38
NC_000007.13:g.40039028A>C , CM000669.1:g.40039028A>C GRCh37
NC_000007.12:g.40005553A>C NCBI36
NG_052965.1:g.54070A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000181839.10:c.2111A>C MANE Select ENSP00000181839.4:p.Lys704Thr
ENST00000340829.10:c.2111A>C ENSP00000340557.5:p.Lys704Thr
ENST00000484589.2:c.663A>C
ENST00000642213.1:n.593A>C
ENST00000643859.1:c.1002A>C
ENST00000643915.1:c.425A>C ENSP00000496187.1:p.Lys142Thr
ENST00000645470.1:c.41A>C ENSP00000495036.1:p.Lys14Thr
ENST00000646039.1:c.1451A>C ENSP00000494168.1:p.Lys484Thr
ENST00000646437.1:c.745A>C
ENST00000647453.1:n.1180A>C
ENST00000647518.1:n.3948A>C
ENST00000181839.8:c.2111A>C ENSP00000181839.4:p.Lys704Thr
ENST00000340829.9:c.2111A>C ENSP00000340557.5:p.Lys704Thr
ENST00000484589.1:n.663A>C
ENST00000611390.1:c.269A>C ENSP00000484610.1:p.Lys90Thr
ENST00000613626.4:c.269A>C ENSP00000480835.1:p.Lys90Thr
NM_003718.4:c.2111A>C NP_003709.3:p.Lys704Thr
NM_031267.3:c.2111A>C NP_112557.2:p.Lys704Thr
XM_011515597.1:c.2111A>C XP_011513899.1:p.Lys704Thr
XM_011515598.1:c.2111A>C XP_011513900.1:p.Lys704Thr
XM_011515597.3:c.2111A>C XP_011513899.1:p.Lys704Thr
XM_017012750.2:c.2111A>C XP_016868239.1:p.Lys704Thr
XM_017012751.2:c.2111A>C XP_016868240.1:p.Lys704Thr
NM_003718.5:c.2111A>C MANE Select NP_003709.3:p.Lys704Thr