Canonical Allele Identifier: CA367280489
Gene: CDK13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40046018A>T , CM000669.2:g.40046018A>T GRCh38
NC_000007.13:g.40085617A>T , CM000669.1:g.40085617A>T GRCh37
NC_000007.12:g.40052142A>T NCBI36
NG_052965.1:g.100659A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700485.1:n.272A>T
ENST00000700486.1:n.310A>T
ENST00000700487.1:n.278A>T
ENST00000181839.10:c.2536A>T MANE Select ENSP00000181839.4:p.Asn846Tyr
ENST00000340829.10:c.2536A>T ENSP00000340557.5:p.Asn846Tyr
ENST00000484589.2:c.1088A>T
ENST00000642592.1:c.89A>T
ENST00000643859.1:c.1427A>T
ENST00000643915.1:c.850A>T ENSP00000496187.1:p.Asn284Tyr
ENST00000645470.1:c.466A>T ENSP00000495036.1:p.Asn156Tyr
ENST00000646039.1:c.1876A>T ENSP00000494168.1:p.Asn626Tyr
ENST00000647453.1:n.1605A>T
ENST00000181839.8:c.2536A>T ENSP00000181839.4:p.Asn846Tyr
ENST00000340829.9:c.2536A>T ENSP00000340557.5:p.Asn846Tyr
ENST00000484589.1:n.1088A>T
ENST00000611390.1:c.694A>T ENSP00000484610.1:p.Asn232Tyr
ENST00000613626.4:c.694A>T ENSP00000480835.1:p.Asn232Tyr
NM_003718.4:c.2536A>T NP_003709.3:p.Asn846Tyr
NM_031267.3:c.2536A>T NP_112557.2:p.Asn846Tyr
XM_011515597.1:c.2536A>T XP_011513899.1:p.Asn846Tyr
XM_011515598.1:c.2536A>T XP_011513900.1:p.Asn846Tyr
XM_011515597.3:c.2536A>T XP_011513899.1:p.Asn846Tyr
XM_017012750.2:c.2536A>T XP_016868239.1:p.Asn846Tyr
XM_017012751.2:c.2536A>T XP_016868240.1:p.Asn846Tyr
NM_003718.5:c.2536A>T MANE Select NP_003709.3:p.Asn846Tyr