Canonical Allele Identifier: CA2775131549

Gene: CDK13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999538_39999539insCTG , CM000669.2:g.39999538_39999539insCTG	GRCh38
NC_000007.13:g.40039137_40039138insCTG , CM000669.1:g.40039137_40039138insCTG	GRCh37
NC_000007.12:g.40005662_40005663insCTG	NCBI36
NG_052965.1:g.54179_54180insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2182+38_2182+39insCTG MANE Select	ENSP00000181839.4:n.2182+38_2182+39insCTG
ENST00000340829.10:c.2182+38_2182+39insCTG	ENSP00000340557.5:n.2182+38_2182+39insCTG
ENST00000484589.2:c.734+38_734+39insCTG
ENST00000642213.1:n.664+38_664+39insCTG
ENST00000643859.1:c.1073+38_1073+39insCTG
ENST00000643915.1:c.496+38_496+39insCTG	ENSP00000496187.1:n.496+38_496+39insCTG
ENST00000645470.1:c.112+38_112+39insCTG	ENSP00000495036.1:n.112+38_112+39insCTG
ENST00000646039.1:c.1522+38_1522+39insCTG	ENSP00000494168.1:n.1522+38_1522+39insCTG
ENST00000647453.1:n.1251+38_1251+39insCTG
ENST00000647518.1:n.4019+38_4019+39insCTG
ENST00000181839.8:c.2182+38_2182+39insCTG	ENSP00000181839.4:n.2182+38_2182+39insCTG
ENST00000340829.9:c.2182+38_2182+39insCTG	ENSP00000340557.5:n.2182+38_2182+39insCTG
ENST00000484589.1:n.734+38_734+39insCTG
ENST00000611390.1:c.340+38_340+39insCTG	ENSP00000484610.1:n.340+38_340+39insCTG
ENST00000613626.4:c.340+38_340+39insCTG	ENSP00000480835.1:n.340+38_340+39insCTG
NM_003718.4:c.2182+38_2182+39insCTG	NP_003709.3:n.2182+38_2182+39insCTG
NM_031267.3:c.2182+38_2182+39insCTG	NP_112557.2:n.2182+38_2182+39insCTG
XM_011515597.1:c.2182+38_2182+39insCTG	XP_011513899.1:n.2182+38_2182+39insCTG
XM_011515598.1:c.2182+38_2182+39insCTG	XP_011513900.1:n.2182+38_2182+39insCTG
XM_011515597.3:c.2182+38_2182+39insCTG	XP_011513899.1:n.2182+38_2182+39insCTG
XM_017012750.2:c.2182+38_2182+39insCTG	XP_016868239.1:n.2182+38_2182+39insCTG
XM_017012751.2:c.2182+38_2182+39insCTG	XP_016868240.1:n.2182+38_2182+39insCTG
NM_003718.5:c.2182+38_2182+39insCTG MANE Select	NP_003709.3:n.2182+38_2182+39insCTG