Canonical Allele Identifier: CA1701739460
Gene: CDK13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40001930G= , CM000669.2:g.40001930G= GRCh38
NC_000007.13:g.40041529G= , CM000669.1:g.40041529G= GRCh37
NC_000007.12:g.40008054G= NCBI36
NG_052965.1:g.56571G=

Transcript Alleles

HGVS Amino-acid change
ENST00000181839.10:c.2252G= MANE Select ENSP00000181839.4:p.Arg751=
ENST00000340829.10:c.2252G= ENSP00000340557.5:p.Arg751=
ENST00000484589.2:c.804G=
ENST00000642213.1:n.734G=
ENST00000643859.1:c.1143G=
ENST00000643915.1:c.566G= ENSP00000496187.1:p.Arg189=
ENST00000645470.1:c.182G= ENSP00000495036.1:p.Arg61=
ENST00000646039.1:c.1592G= ENSP00000494168.1:p.Arg531=
ENST00000647453.1:n.1321G=
ENST00000647518.1:n.4089G=
ENST00000181839.8:c.2252G= ENSP00000181839.4:p.Arg751=
ENST00000340829.9:c.2252G= ENSP00000340557.5:p.Arg751=
ENST00000484589.1:n.804G=
ENST00000611390.1:c.410G= ENSP00000484610.1:p.Arg137=
ENST00000613626.4:c.410G= ENSP00000480835.1:p.Arg137=
NM_003718.4:c.2252G= NP_003709.3:p.Arg751=
NM_031267.3:c.2252G= NP_112557.2:p.Arg751=
XM_011515597.1:c.2252G= XP_011513899.1:p.Arg751=
XM_011515598.1:c.2252G= XP_011513900.1:p.Arg751=
XM_011515597.3:c.2252G= XP_011513899.1:p.Arg751=
XM_017012750.2:c.2252G= XP_016868239.1:p.Arg751=
XM_017012751.2:c.2252G= XP_016868240.1:p.Arg751=
NM_003718.5:c.2252G= MANE Select NP_003709.3:p.Arg751=