Canonical Allele Identifier: CA1701739461
Gene: CDK13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40001935A= , CM000669.2:g.40001935A= GRCh38
NC_000007.13:g.40041534A= , CM000669.1:g.40041534A= GRCh37
NC_000007.12:g.40008059A= NCBI36
NG_052965.1:g.56576A=

Transcript Alleles

HGVS Amino-acid change
ENST00000181839.10:c.2257A= MANE Select ENSP00000181839.4:p.Ile753=
ENST00000340829.10:c.2257A= ENSP00000340557.5:p.Ile753=
ENST00000484589.2:c.809A=
ENST00000642213.1:n.739A=
ENST00000643859.1:c.1148A=
ENST00000643915.1:c.571A= ENSP00000496187.1:p.Ile191=
ENST00000645470.1:c.187A= ENSP00000495036.1:p.Ile63=
ENST00000646039.1:c.1597A= ENSP00000494168.1:p.Ile533=
ENST00000647453.1:n.1326A=
ENST00000647518.1:n.4094A=
ENST00000181839.8:c.2257A= ENSP00000181839.4:p.Ile753=
ENST00000340829.9:c.2257A= ENSP00000340557.5:p.Ile753=
ENST00000484589.1:n.809A=
ENST00000611390.1:c.415A= ENSP00000484610.1:p.Ile139=
ENST00000613626.4:c.415A= ENSP00000480835.1:p.Ile139=
NM_003718.4:c.2257A= NP_003709.3:p.Ile753=
NM_031267.3:c.2257A= NP_112557.2:p.Ile753=
XM_011515597.1:c.2257A= XP_011513899.1:p.Ile753=
XM_011515598.1:c.2257A= XP_011513900.1:p.Ile753=
XM_011515597.3:c.2257A= XP_011513899.1:p.Ile753=
XM_017012750.2:c.2257A= XP_016868239.1:p.Ile753=
XM_017012751.2:c.2257A= XP_016868240.1:p.Ile753=
NM_003718.5:c.2257A= MANE Select NP_003709.3:p.Ile753=