Canonical Allele Identifier: CA2682487101

Gene: CDK13

Linked Data

• gnomAD v4: 7-39999479-AAAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999480_39999482del , CM000669.2:g.39999480_39999482del	GRCh38
NC_000007.13:g.40039079_40039081del , CM000669.1:g.40039079_40039081del	GRCh37
NC_000007.12:g.40005604_40005606del	NCBI36
NG_052965.1:g.54121_54123del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2162_2164del MANE Select	ENSP00000181839.4:p.Lys721_Ala722delinsThr
ENST00000340829.10:c.2162_2164del	ENSP00000340557.5:p.Lys721_Ala722delinsThr
ENST00000484589.2:c.714_716del
ENST00000642213.1:n.644_646del
ENST00000643859.1:c.1053_1055del
ENST00000643915.1:c.476_478del	ENSP00000496187.1:p.Lys159_Ala160delinsThr
ENST00000645470.1:c.92_94del	ENSP00000495036.1:p.Lys31_Ala32delinsThr
ENST00000646039.1:c.1502_1504del	ENSP00000494168.1:p.Lys501_Ala502delinsThr
ENST00000647453.1:n.1231_1233del
ENST00000647518.1:n.3999_4001del
ENST00000181839.8:c.2162_2164del	ENSP00000181839.4:p.Lys721_Ala722delinsThr
ENST00000340829.9:c.2162_2164del	ENSP00000340557.5:p.Lys721_Ala722delinsThr
ENST00000484589.1:n.714_716del
ENST00000611390.1:c.320_322del	ENSP00000484610.1:p.Lys107_Ala108delinsThr
ENST00000613626.4:c.320_322del	ENSP00000480835.1:p.Lys107_Ala108delinsThr
NM_003718.4:c.2162_2164del	NP_003709.3:p.Lys721_Ala722delinsThr
NM_031267.3:c.2162_2164del	NP_112557.2:p.Lys721_Ala722delinsThr
XM_011515597.1:c.2162_2164del	XP_011513899.1:p.Lys721_Ala722delinsThr
XM_011515598.1:c.2162_2164del	XP_011513900.1:p.Lys721_Ala722delinsThr
XM_011515597.3:c.2162_2164del	XP_011513899.1:p.Lys721_Ala722delinsThr
XM_017012750.2:c.2162_2164del	XP_016868239.1:p.Lys721_Ala722delinsThr
XM_017012751.2:c.2162_2164del	XP_016868240.1:p.Lys721_Ala722delinsThr
NM_003718.5:c.2162_2164del MANE Select	NP_003709.3:p.Lys721_Ala722delinsThr