Canonical Allele Identifier: CA367287961
Gene: CDK13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.39999365T>A , CM000669.2:g.39999365T>A GRCh38
NC_000007.13:g.40038964T>A , CM000669.1:g.40038964T>A GRCh37
NC_000007.12:g.40005489T>A NCBI36
NG_052965.1:g.54006T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000181839.10:c.2047T>A MANE Select ENSP00000181839.4:p.Cys683Ser
ENST00000340829.10:c.2047T>A ENSP00000340557.5:p.Cys683Ser
ENST00000484589.2:c.599T>A
ENST00000642213.1:n.529T>A
ENST00000642660.1:n.927T>A
ENST00000643859.1:c.938T>A
ENST00000643915.1:c.361T>A ENSP00000496187.1:p.Cys121Ser
ENST00000646039.1:c.1387T>A ENSP00000494168.1:p.Cys463Ser
ENST00000646437.1:c.681T>A
ENST00000647453.1:n.1116T>A
ENST00000647518.1:n.3884T>A
ENST00000181839.8:c.2047T>A ENSP00000181839.4:p.Cys683Ser
ENST00000340829.9:c.2047T>A ENSP00000340557.5:p.Cys683Ser
ENST00000484589.1:n.599T>A
ENST00000611390.1:c.205T>A ENSP00000484610.1:p.Cys69Ser
ENST00000613626.4:c.205T>A ENSP00000480835.1:p.Cys69Ser
NM_003718.4:c.2047T>A NP_003709.3:p.Cys683Ser
NM_031267.3:c.2047T>A NP_112557.2:p.Cys683Ser
XM_011515597.1:c.2047T>A XP_011513899.1:p.Cys683Ser
XM_011515598.1:c.2047T>A XP_011513900.1:p.Cys683Ser
XM_011515597.3:c.2047T>A XP_011513899.1:p.Cys683Ser
XM_017012750.2:c.2047T>A XP_016868239.1:p.Cys683Ser
XM_017012751.2:c.2047T>A XP_016868240.1:p.Cys683Ser
NM_003718.5:c.2047T>A MANE Select NP_003709.3:p.Cys683Ser