Canonical Allele Identifier: CA2500181485

Gene: CDK13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.40001855_40001856insCT , CM000669.2:g.40001855_40001856insCT	GRCh38
NC_000007.13:g.40041454_40041455insCT , CM000669.1:g.40041454_40041455insCT	GRCh37
NC_000007.12:g.40007979_40007980insCT	NCBI36
NG_052965.1:g.56496_56497insCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000181839.10:c.2183-6_2183-5insCT MANE Select	ENSP00000181839.4:n.2183-6_2183-5insCT
ENST00000340829.10:c.2183-6_2183-5insCT	ENSP00000340557.5:n.2183-6_2183-5insCT
ENST00000484589.2:c.735-6_735-5insCT
ENST00000642213.1:n.665-6_665-5insCT
ENST00000643859.1:c.1074-6_1074-5insCT
ENST00000643915.1:c.497-6_497-5insCT	ENSP00000496187.1:n.497-6_497-5insCT
ENST00000645470.1:c.113-6_113-5insCT	ENSP00000495036.1:n.113-6_113-5insCT
ENST00000646039.1:c.1523-6_1523-5insCT	ENSP00000494168.1:n.1523-6_1523-5insCT
ENST00000647453.1:n.1252-6_1252-5insCT
ENST00000647518.1:n.4020-6_4020-5insCT
ENST00000181839.8:c.2183-6_2183-5insCT	ENSP00000181839.4:n.2183-6_2183-5insCT
ENST00000340829.9:c.2183-6_2183-5insCT	ENSP00000340557.5:n.2183-6_2183-5insCT
ENST00000484589.1:n.735-6_735-5insCT
ENST00000611390.1:c.341-6_341-5insCT	ENSP00000484610.1:n.341-6_341-5insCT
ENST00000613626.4:c.341-6_341-5insCT	ENSP00000480835.1:n.341-6_341-5insCT
NM_003718.4:c.2183-6_2183-5insCT	NP_003709.3:n.2183-6_2183-5insCT
NM_031267.3:c.2183-6_2183-5insCT	NP_112557.2:n.2183-6_2183-5insCT
XM_011515597.1:c.2183-6_2183-5insCT	XP_011513899.1:n.2183-6_2183-5insCT
XM_011515598.1:c.2183-6_2183-5insCT	XP_011513900.1:n.2183-6_2183-5insCT
XM_011515597.3:c.2183-6_2183-5insCT	XP_011513899.1:n.2183-6_2183-5insCT
XM_017012750.2:c.2183-6_2183-5insCT	XP_016868239.1:n.2183-6_2183-5insCT
XM_017012751.2:c.2183-6_2183-5insCT	XP_016868240.1:n.2183-6_2183-5insCT
NM_003718.5:c.2183-6_2183-5insCT MANE Select	NP_003709.3:n.2183-6_2183-5insCT