Canonical Allele Identifier: CA367288087

Gene: CDK13

Linked Data

• COSMIC: COSM4671092
• MyVariant Identifiers: chr7:g.40039004A>G (hg19) ; chr7:g.39999405A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999405A>G , CM000669.2:g.39999405A>G	GRCh38
NC_000007.13:g.40039004A>G , CM000669.1:g.40039004A>G	GRCh37
NC_000007.12:g.40005529A>G	NCBI36
NG_052965.1:g.54046A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2087A>G MANE Select	ENSP00000181839.4:p.Asp696Gly
ENST00000340829.10:c.2087A>G	ENSP00000340557.5:p.Asp696Gly
ENST00000484589.2:c.639A>G
ENST00000642213.1:n.569A>G
ENST00000643859.1:c.978A>G
ENST00000643915.1:c.401A>G	ENSP00000496187.1:p.Asp134Gly
ENST00000645470.1:c.17A>G	ENSP00000495036.1:p.Asp6Gly
ENST00000646039.1:c.1427A>G	ENSP00000494168.1:p.Asp476Gly
ENST00000646437.1:c.721A>G
ENST00000647453.1:n.1156A>G
ENST00000647518.1:n.3924A>G
ENST00000181839.8:c.2087A>G	ENSP00000181839.4:p.Asp696Gly
ENST00000340829.9:c.2087A>G	ENSP00000340557.5:p.Asp696Gly
ENST00000484589.1:n.639A>G
ENST00000611390.1:c.245A>G	ENSP00000484610.1:p.Asp82Gly
ENST00000613626.4:c.245A>G	ENSP00000480835.1:p.Asp82Gly
NM_003718.4:c.2087A>G	NP_003709.3:p.Asp696Gly
NM_031267.3:c.2087A>G	NP_112557.2:p.Asp696Gly
XM_011515597.1:c.2087A>G	XP_011513899.1:p.Asp696Gly
XM_011515598.1:c.2087A>G	XP_011513900.1:p.Asp696Gly
XM_011515597.3:c.2087A>G	XP_011513899.1:p.Asp696Gly
XM_017012750.2:c.2087A>G	XP_016868239.1:p.Asp696Gly
XM_017012751.2:c.2087A>G	XP_016868240.1:p.Asp696Gly
NM_003718.5:c.2087A>G MANE Select	NP_003709.3:p.Asp696Gly