Canonical Allele Identifier: CA16044433
Gene: CDK13 HGNC NCBI

Linked Data

ClinVar Variation Id: 375738
ClinVar RCV Id: RCV000417209
dbSNP Id: rs1057519633

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.39999458G>C , CM000669.2:g.39999458G>C GRCh38
NC_000007.13:g.40039057G>C , CM000669.1:g.40039057G>C GRCh37
NC_000007.12:g.40005582G>C NCBI36
NG_052965.1:g.54099G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000181839.10:c.2140G>C MANE Select ENSP00000181839.4:p.Gly714Arg
ENST00000340829.10:c.2140G>C ENSP00000340557.5:p.Gly714Arg
ENST00000484589.2:c.692G>C
ENST00000642213.1:n.622G>C
ENST00000643859.1:c.1031G>C
ENST00000643915.1:c.454G>C ENSP00000496187.1:p.Gly152Arg
ENST00000645470.1:c.70G>C ENSP00000495036.1:p.Gly24Arg
ENST00000646039.1:c.1480G>C ENSP00000494168.1:p.Gly494Arg
ENST00000647453.1:n.1209G>C
ENST00000647518.1:n.3977G>C
ENST00000181839.8:c.2140G>C ENSP00000181839.4:p.Gly714Arg
ENST00000340829.9:c.2140G>C ENSP00000340557.5:p.Gly714Arg
ENST00000484589.1:n.692G>C
ENST00000611390.1:c.298G>C ENSP00000484610.1:p.Gly100Arg
ENST00000613626.4:c.298G>C ENSP00000480835.1:p.Gly100Arg
NM_003718.4:c.2140G>C NP_003709.3:p.Gly714Arg
NM_031267.3:c.2140G>C NP_112557.2:p.Gly714Arg
XM_011515597.1:c.2140G>C XP_011513899.1:p.Gly714Arg
XM_011515598.1:c.2140G>C XP_011513900.1:p.Gly714Arg
XM_011515597.3:c.2140G>C XP_011513899.1:p.Gly714Arg
XM_017012750.2:c.2140G>C XP_016868239.1:p.Gly714Arg
XM_017012751.2:c.2140G>C XP_016868240.1:p.Gly714Arg
NM_003718.5:c.2140G>C MANE Select NP_003709.3:p.Gly714Arg