Canonical Allele Identifier: CA367288398
Gene: CDK13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.39999470C>A , CM000669.2:g.39999470C>A GRCh38
NC_000007.13:g.40039069C>A , CM000669.1:g.40039069C>A GRCh37
NC_000007.12:g.40005594C>A NCBI36
NG_052965.1:g.54111C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000181839.10:c.2152C>A MANE Select ENSP00000181839.4:p.Gln718Lys
ENST00000340829.10:c.2152C>A ENSP00000340557.5:p.Gln718Lys
ENST00000484589.2:c.704C>A
ENST00000642213.1:n.634C>A
ENST00000643859.1:c.1043C>A
ENST00000643915.1:c.466C>A ENSP00000496187.1:p.Gln156Lys
ENST00000645470.1:c.82C>A ENSP00000495036.1:p.Gln28Lys
ENST00000646039.1:c.1492C>A ENSP00000494168.1:p.Gln498Lys
ENST00000647453.1:n.1221C>A
ENST00000647518.1:n.3989C>A
ENST00000181839.8:c.2152C>A ENSP00000181839.4:p.Gln718Lys
ENST00000340829.9:c.2152C>A ENSP00000340557.5:p.Gln718Lys
ENST00000484589.1:n.704C>A
ENST00000611390.1:c.310C>A ENSP00000484610.1:p.Gln104Lys
ENST00000613626.4:c.310C>A ENSP00000480835.1:p.Gln104Lys
NM_003718.4:c.2152C>A NP_003709.3:p.Gln718Lys
NM_031267.3:c.2152C>A NP_112557.2:p.Gln718Lys
XM_011515597.1:c.2152C>A XP_011513899.1:p.Gln718Lys
XM_011515598.1:c.2152C>A XP_011513900.1:p.Gln718Lys
XM_011515597.3:c.2152C>A XP_011513899.1:p.Gln718Lys
XM_017012750.2:c.2152C>A XP_016868239.1:p.Gln718Lys
XM_017012751.2:c.2152C>A XP_016868240.1:p.Gln718Lys
NM_003718.5:c.2152C>A MANE Select NP_003709.3:p.Gln718Lys