Canonical Allele Identifier: CA2546699677

Gene: CDK13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999812_39999813insATCACAAATACTAAAGGAACACTTTTTAAAATAT , CM000669.2:g.39999812_39999813insATCACAAATACTAAAGGAACACTTTTTAAAATAT	GRCh38
NC_000007.13:g.40039411_40039412insATCACAAATACTAAAGGAACACTTTTTAAAATAT , CM000669.1:g.40039411_40039412insATCACAAATACTAAAGGAACACTTTTTAAAATAT	GRCh37
NC_000007.12:g.40005936_40005937insATCACAAATACTAAAGGAACACTTTTTAAAATAT	NCBI36
NG_052965.1:g.54453_54454insATCACAAATACTAAAGGAACACTTTTTAAAATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2182+312_2182+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT MANE Select	ENSP00000181839.4:n.2182+312_2182+313insATCACAAATACTAAAGGAACA...
ENST00000340829.10:c.2182+312_2182+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT	ENSP00000340557.5:n.2182+312_2182+313insATCACAAATACTAAAGGAACA...
ENST00000484589.2:c.734+312_734+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT
ENST00000642213.1:n.664+312_664+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT
ENST00000643859.1:c.1073+312_1073+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT
ENST00000643915.1:c.496+312_496+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT	ENSP00000496187.1:n.496+312_496+313insATCACAAATACTAAAGGAACACT...
ENST00000645470.1:c.112+312_112+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT	ENSP00000495036.1:n.112+312_112+313insATCACAAATACTAAAGGAACACT...
ENST00000646039.1:c.1522+312_1522+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT	ENSP00000494168.1:n.1522+312_1522+313insATCACAAATACTAAAGGAACA...
ENST00000647453.1:n.1251+312_1251+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT
ENST00000647518.1:n.4019+312_4019+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT
ENST00000181839.8:c.2182+312_2182+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT	ENSP00000181839.4:n.2182+312_2182+313insATCACAAATACTAAAGGAACA...
ENST00000340829.9:c.2182+312_2182+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT	ENSP00000340557.5:n.2182+312_2182+313insATCACAAATACTAAAGGAACA...
ENST00000484589.1:n.734+312_734+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT
ENST00000611390.1:c.340+312_340+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT	ENSP00000484610.1:n.340+312_340+313insATCACAAATACTAAAGGAACACT...
ENST00000613626.4:c.340+312_340+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT	ENSP00000480835.1:n.340+312_340+313insATCACAAATACTAAAGGAACACT...
NM_003718.4:c.2182+312_2182+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT	NP_003709.3:n.2182+312_2182+313insATCACAAATACTAAAGGAACACTTTTT...
NM_031267.3:c.2182+312_2182+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT	NP_112557.2:n.2182+312_2182+313insATCACAAATACTAAAGGAACACTTTTT...
XM_011515597.1:c.2182+312_2182+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT	XP_011513899.1:n.2182+312_2182+313insATCACAAATACTAAAGGAACACTT...
XM_011515598.1:c.2182+312_2182+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT	XP_011513900.1:n.2182+312_2182+313insATCACAAATACTAAAGGAACACTT...
XM_011515597.3:c.2182+312_2182+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT	XP_011513899.1:n.2182+312_2182+313insATCACAAATACTAAAGGAACACTT...
XM_017012750.2:c.2182+312_2182+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT	XP_016868239.1:n.2182+312_2182+313insATCACAAATACTAAAGGAACACTT...
XM_017012751.2:c.2182+312_2182+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT	XP_016868240.1:n.2182+312_2182+313insATCACAAATACTAAAGGAACACTT...
NM_003718.5:c.2182+312_2182+313insATCACAAATACTAAAGGAACACTTTTTAAAATAT MANE Select	NP_003709.3:n.2182+312_2182+313insATCACAAATACTAAAGGAACACTTTTT...