Canonical Allele Identifier: CA367288120
Gene: CDK13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.39999414A>T , CM000669.2:g.39999414A>T GRCh38
NC_000007.13:g.40039013A>T , CM000669.1:g.40039013A>T GRCh37
NC_000007.12:g.40005538A>T NCBI36
NG_052965.1:g.54055A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000181839.10:c.2096A>T MANE Select ENSP00000181839.4:p.Lys699Ile
ENST00000340829.10:c.2096A>T ENSP00000340557.5:p.Lys699Ile
ENST00000484589.2:c.648A>T
ENST00000642213.1:n.578A>T
ENST00000643859.1:c.987A>T
ENST00000643915.1:c.410A>T ENSP00000496187.1:p.Lys137Ile
ENST00000645470.1:c.26A>T ENSP00000495036.1:p.Lys9Ile
ENST00000646039.1:c.1436A>T ENSP00000494168.1:p.Lys479Ile
ENST00000646437.1:c.730A>T
ENST00000647453.1:n.1165A>T
ENST00000647518.1:n.3933A>T
ENST00000181839.8:c.2096A>T ENSP00000181839.4:p.Lys699Ile
ENST00000340829.9:c.2096A>T ENSP00000340557.5:p.Lys699Ile
ENST00000484589.1:n.648A>T
ENST00000611390.1:c.254A>T ENSP00000484610.1:p.Lys85Ile
ENST00000613626.4:c.254A>T ENSP00000480835.1:p.Lys85Ile
NM_003718.4:c.2096A>T NP_003709.3:p.Lys699Ile
NM_031267.3:c.2096A>T NP_112557.2:p.Lys699Ile
XM_011515597.1:c.2096A>T XP_011513899.1:p.Lys699Ile
XM_011515598.1:c.2096A>T XP_011513900.1:p.Lys699Ile
XM_011515597.3:c.2096A>T XP_011513899.1:p.Lys699Ile
XM_017012750.2:c.2096A>T XP_016868239.1:p.Lys699Ile
XM_017012751.2:c.2096A>T XP_016868240.1:p.Lys699Ile
NM_003718.5:c.2096A>T MANE Select NP_003709.3:p.Lys699Ile