Canonical Allele Identifier: CA16618457
Gene: CDK13 HGNC NCBI

Linked Data

ClinVar Variation Id: 422362
dbSNP Id: rs1064795731

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40001878A>G , CM000669.2:g.40001878A>G GRCh38
NC_000007.13:g.40041477A>G , CM000669.1:g.40041477A>G GRCh37
NC_000007.12:g.40008002A>G NCBI36
NG_052965.1:g.56519A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000181839.10:c.2200A>G MANE Select ENSP00000181839.4:p.Lys734Glu
ENST00000340829.10:c.2200A>G ENSP00000340557.5:p.Lys734Glu
ENST00000484589.2:c.752A>G
ENST00000642213.1:n.682A>G
ENST00000643859.1:c.1091A>G
ENST00000643915.1:c.514A>G ENSP00000496187.1:p.Lys172Glu
ENST00000645470.1:c.130A>G ENSP00000495036.1:p.Lys44Glu
ENST00000646039.1:c.1540A>G ENSP00000494168.1:p.Lys514Glu
ENST00000647453.1:n.1269A>G
ENST00000647518.1:n.4037A>G
ENST00000181839.8:c.2200A>G ENSP00000181839.4:p.Lys734Glu
ENST00000340829.9:c.2200A>G ENSP00000340557.5:p.Lys734Glu
ENST00000484589.1:n.752A>G
ENST00000611390.1:c.358A>G ENSP00000484610.1:p.Lys120Glu
ENST00000613626.4:c.358A>G ENSP00000480835.1:p.Lys120Glu
NM_003718.4:c.2200A>G NP_003709.3:p.Lys734Glu
NM_031267.3:c.2200A>G NP_112557.2:p.Lys734Glu
XM_011515597.1:c.2200A>G XP_011513899.1:p.Lys734Glu
XM_011515598.1:c.2200A>G XP_011513900.1:p.Lys734Glu
XM_011515597.3:c.2200A>G XP_011513899.1:p.Lys734Glu
XM_017012750.2:c.2200A>G XP_016868239.1:p.Lys734Glu
XM_017012751.2:c.2200A>G XP_016868240.1:p.Lys734Glu
NM_003718.5:c.2200A>G MANE Select NP_003709.3:p.Lys734Glu