Canonical Allele Identifier: CA367287993
Gene: CDK13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.39999379T>A , CM000669.2:g.39999379T>A GRCh38
NC_000007.13:g.40038978T>A , CM000669.1:g.40038978T>A GRCh37
NC_000007.12:g.40005503T>A NCBI36
NG_052965.1:g.54020T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000181839.10:c.2061T>A MANE Select ENSP00000181839.4:p.Tyr687Ter
ENST00000340829.10:c.2061T>A ENSP00000340557.5:p.Tyr687Ter
ENST00000484589.2:c.613T>A
ENST00000642213.1:n.543T>A
ENST00000642660.1:n.941T>A
ENST00000643859.1:c.952T>A
ENST00000643915.1:c.375T>A ENSP00000496187.1:p.Tyr125Ter
ENST00000646039.1:c.1401T>A ENSP00000494168.1:p.Tyr467Ter
ENST00000646437.1:c.695T>A
ENST00000647453.1:n.1130T>A
ENST00000647518.1:n.3898T>A
ENST00000181839.8:c.2061T>A ENSP00000181839.4:p.Tyr687Ter
ENST00000340829.9:c.2061T>A ENSP00000340557.5:p.Tyr687Ter
ENST00000484589.1:n.613T>A
ENST00000611390.1:c.219T>A ENSP00000484610.1:p.Tyr73Ter
ENST00000613626.4:c.219T>A ENSP00000480835.1:p.Tyr73Ter
NM_003718.4:c.2061T>A NP_003709.3:p.Tyr687Ter
NM_031267.3:c.2061T>A NP_112557.2:p.Tyr687Ter
XM_011515597.1:c.2061T>A XP_011513899.1:p.Tyr687Ter
XM_011515598.1:c.2061T>A XP_011513900.1:p.Tyr687Ter
XM_011515597.3:c.2061T>A XP_011513899.1:p.Tyr687Ter
XM_017012750.2:c.2061T>A XP_016868239.1:p.Tyr687Ter
XM_017012751.2:c.2061T>A XP_016868240.1:p.Tyr687Ter
NM_003718.5:c.2061T>A MANE Select NP_003709.3:p.Tyr687Ter