Canonical Allele Identifier: CA1701739437
Gene: CDK13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40001837T= , CM000669.2:g.40001837T= GRCh38
NC_000007.13:g.40041436T= , CM000669.1:g.40041436T= GRCh37
NC_000007.12:g.40007961T= NCBI36
NG_052965.1:g.56478T=

Transcript Alleles

HGVS Amino-acid change
ENST00000181839.10:c.2183-24T= MANE Select ENSP00000181839.4:n.2183-24T=
ENST00000340829.10:c.2183-24T= ENSP00000340557.5:n.2183-24T=
ENST00000484589.2:c.735-24T=
ENST00000642213.1:n.665-24T=
ENST00000643859.1:c.1074-24T=
ENST00000643915.1:c.497-24T= ENSP00000496187.1:n.497-24T=
ENST00000645470.1:c.113-24T= ENSP00000495036.1:n.113-24T=
ENST00000646039.1:c.1523-24T= ENSP00000494168.1:n.1523-24T=
ENST00000647453.1:n.1252-24T=
ENST00000647518.1:n.4020-24T=
ENST00000181839.8:c.2183-24T= ENSP00000181839.4:n.2183-24T=
ENST00000340829.9:c.2183-24T= ENSP00000340557.5:n.2183-24T=
ENST00000484589.1:n.735-24T=
ENST00000611390.1:c.341-24T= ENSP00000484610.1:n.341-24T=
ENST00000613626.4:c.341-24T= ENSP00000480835.1:n.341-24T=
NM_003718.4:c.2183-24T= NP_003709.3:n.2183-24T=
NM_031267.3:c.2183-24T= NP_112557.2:n.2183-24T=
XM_011515597.1:c.2183-24T= XP_011513899.1:n.2183-24T=
XM_011515598.1:c.2183-24T= XP_011513900.1:n.2183-24T=
XM_011515597.3:c.2183-24T= XP_011513899.1:n.2183-24T=
XM_017012750.2:c.2183-24T= XP_016868239.1:n.2183-24T=
XM_017012751.2:c.2183-24T= XP_016868240.1:n.2183-24T=
NM_003718.5:c.2183-24T= MANE Select NP_003709.3:n.2183-24T=