Canonical Allele Identifier: CA1701739440

Gene: CDK13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.40001853_40001854delinsCT , CM000669.2:g.40001853_40001854delinsCT	GRCh38
NC_000007.13:g.40041452_40041453delinsCT , CM000669.1:g.40041452_40041453delinsCT	GRCh37
NC_000007.12:g.40007977_40007978delinsCT	NCBI36
NG_052965.1:g.56494_56495delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000181839.10:c.2183-8_2183-7delinsCT MANE Select	ENSP00000181839.4:n.2183-8_2183-7delinsCT...
ENST00000340829.10:c.2183-8_2183-7delinsCT	ENSP00000340557.5:n.2183-8_2183-7delinsCT...
ENST00000484589.2:c.735-8_735-7delinsCT
ENST00000642213.1:n.665-8_665-7delinsCT
ENST00000643859.1:c.1074-8_1074-7delinsCT
ENST00000643915.1:c.497-8_497-7delinsCT	ENSP00000496187.1:n.497-8_497-7delinsCT
ENST00000645470.1:c.113-8_113-7delinsCT	ENSP00000495036.1:n.113-8_113-7delinsCT
ENST00000646039.1:c.1523-8_1523-7delinsCT	ENSP00000494168.1:n.1523-8_1523-7delinsCT...
ENST00000647453.1:n.1252-8_1252-7delinsCT
ENST00000647518.1:n.4020-8_4020-7delinsCT
ENST00000181839.8:c.2183-8_2183-7delinsCT	ENSP00000181839.4:n.2183-8_2183-7delinsCT...
ENST00000340829.9:c.2183-8_2183-7delinsCT	ENSP00000340557.5:n.2183-8_2183-7delinsCT...
ENST00000484589.1:n.735-8_735-7delinsCT
ENST00000611390.1:c.341-8_341-7delinsCT	ENSP00000484610.1:n.341-8_341-7delinsCT
ENST00000613626.4:c.341-8_341-7delinsCT	ENSP00000480835.1:n.341-8_341-7delinsCT
NM_003718.4:c.2183-8_2183-7delinsCT	NP_003709.3:n.2183-8_2183-7delinsCT
NM_031267.3:c.2183-8_2183-7delinsCT	NP_112557.2:n.2183-8_2183-7delinsCT
XM_011515597.1:c.2183-8_2183-7delinsCT	XP_011513899.1:n.2183-8_2183-7delinsCT
XM_011515598.1:c.2183-8_2183-7delinsCT	XP_011513900.1:n.2183-8_2183-7delinsCT
XM_011515597.3:c.2183-8_2183-7delinsCT	XP_011513899.1:n.2183-8_2183-7delinsCT
XM_017012750.2:c.2183-8_2183-7delinsCT	XP_016868239.1:n.2183-8_2183-7delinsCT
XM_017012751.2:c.2183-8_2183-7delinsCT	XP_016868240.1:n.2183-8_2183-7delinsCT
NM_003718.5:c.2183-8_2183-7delinsCT MANE Select	NP_003709.3:n.2183-8_2183-7delinsCT