Canonical Allele Identifier: CA1701738252

Gene: CDK13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999411_39999412delinsGA , CM000669.2:g.39999411_39999412delinsGA	GRCh38
NC_000007.13:g.40039010_40039011delinsGA , CM000669.1:g.40039010_40039011delinsGA	GRCh37
NC_000007.12:g.40005535_40005536delinsGA	NCBI36
NG_052965.1:g.54052_54053delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2093_2094delinsGA MANE Select	ENSP00000181839.4:p.Gly698=
ENST00000340829.10:c.2093_2094delinsGA	ENSP00000340557.5:p.Gly698=
ENST00000484589.2:c.645_646delinsGA
ENST00000642213.1:n.575_576delinsGA
ENST00000643859.1:c.984_985delinsGA
ENST00000643915.1:c.407_408delinsGA	ENSP00000496187.1:p.Gly136=
ENST00000645470.1:c.23_24delinsGA	ENSP00000495036.1:p.Gly8=
ENST00000646039.1:c.1433_1434delinsGA	ENSP00000494168.1:p.Gly478=
ENST00000646437.1:c.727_728delinsGA
ENST00000647453.1:n.1162_1163delinsGA
ENST00000647518.1:n.3930_3931delinsGA
ENST00000181839.8:c.2093_2094delinsGA	ENSP00000181839.4:p.Gly698=
ENST00000340829.9:c.2093_2094delinsGA	ENSP00000340557.5:p.Gly698=
ENST00000484589.1:n.645_646delinsGA
ENST00000611390.1:c.251_252delinsGA	ENSP00000484610.1:p.Gly84=
ENST00000613626.4:c.251_252delinsGA	ENSP00000480835.1:p.Gly84=
NM_003718.4:c.2093_2094delinsGA	NP_003709.3:p.Gly698=
NM_031267.3:c.2093_2094delinsGA	NP_112557.2:p.Gly698=
XM_011515597.1:c.2093_2094delinsGA	XP_011513899.1:p.Gly698=
XM_011515598.1:c.2093_2094delinsGA	XP_011513900.1:p.Gly698=
XM_011515597.3:c.2093_2094delinsGA	XP_011513899.1:p.Gly698=
XM_017012750.2:c.2093_2094delinsGA	XP_016868239.1:p.Gly698=
XM_017012751.2:c.2093_2094delinsGA	XP_016868240.1:p.Gly698=
NM_003718.5:c.2093_2094delinsGA MANE Select	NP_003709.3:p.Gly698=