Canonical Allele Identifier: CA367288002
Gene: CDK13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.39999383G>T , CM000669.2:g.39999383G>T GRCh38
NC_000007.13:g.40038982G>T , CM000669.1:g.40038982G>T GRCh37
NC_000007.12:g.40005507G>T NCBI36
NG_052965.1:g.54024G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000181839.10:c.2065G>T MANE Select ENSP00000181839.4:p.Glu689Ter
ENST00000340829.10:c.2065G>T ENSP00000340557.5:p.Glu689Ter
ENST00000484589.2:c.617G>T
ENST00000642213.1:n.547G>T
ENST00000642660.1:n.945G>T
ENST00000643859.1:c.956G>T
ENST00000643915.1:c.379G>T ENSP00000496187.1:p.Glu127Ter
ENST00000646039.1:c.1405G>T ENSP00000494168.1:p.Glu469Ter
ENST00000646437.1:c.699G>T
ENST00000647453.1:n.1134G>T
ENST00000647518.1:n.3902G>T
ENST00000181839.8:c.2065G>T ENSP00000181839.4:p.Glu689Ter
ENST00000340829.9:c.2065G>T ENSP00000340557.5:p.Glu689Ter
ENST00000484589.1:n.617G>T
ENST00000611390.1:c.223G>T ENSP00000484610.1:p.Glu75Ter
ENST00000613626.4:c.223G>T ENSP00000480835.1:p.Glu75Ter
NM_003718.4:c.2065G>T NP_003709.3:p.Glu689Ter
NM_031267.3:c.2065G>T NP_112557.2:p.Glu689Ter
XM_011515597.1:c.2065G>T XP_011513899.1:p.Glu689Ter
XM_011515598.1:c.2065G>T XP_011513900.1:p.Glu689Ter
XM_011515597.3:c.2065G>T XP_011513899.1:p.Glu689Ter
XM_017012750.2:c.2065G>T XP_016868239.1:p.Glu689Ter
XM_017012751.2:c.2065G>T XP_016868240.1:p.Glu689Ter
NM_003718.5:c.2065G>T MANE Select NP_003709.3:p.Glu689Ter