Canonical Allele Identifier: CA838355091

Gene: CDK13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39997606_39997608del , CM000669.2:g.39997606_39997608del	GRCh38
NC_000007.13:g.40037205_40037207del , CM000669.1:g.40037205_40037207del	GRCh37
NC_000007.12:g.40003730_40003732del	NCBI36
NG_052965.1:g.52247_52249del

Transcript Alleles

HGVS	Amino-acid Change
NM_003718.5:c.1984_1986del MANE Select	NP_003709.3:p.Ser662del
ENST00000181839.10:c.1984_1986del MANE Select	ENSP00000181839.4:p.Ser662del
NM_003718.4:c.1984_1986del	NP_003709.3:p.Ser662del
NM_031267.3:c.1984_1986del	NP_112557.2:p.Ser662del
ENST00000181839.8:c.1984_1986del	ENSP00000181839.4:p.Ser662del
ENST00000340829.10:c.1984_1986del	ENSP00000340557.5:p.Ser662del
ENST00000340829.9:c.1984_1986del	ENSP00000340557.5:p.Ser662del
ENST00000484589.1:n.536_538del
ENST00000484589.2:c.536_538del
ENST00000611390.1:c.142_144del	ENSP00000484610.1:p.Ser48del
ENST00000613626.4:c.142_144del	ENSP00000480835.1:p.Ser48del
ENST00000642626.1:c.773_775del
ENST00000642660.1:n.773_775del
ENST00000643859.1:c.875_877del
ENST00000643915.1:c.298_300del	ENSP00000496187.1:p.Ser100del
ENST00000646039.1:c.1324_1326del	ENSP00000494168.1:p.Ser442del
ENST00000646437.1:c.603_605del
ENST00000647518.1:n.3821_3823del
XM_011515597.1:c.1984_1986del	XP_011513899.1:p.Ser662del
XM_011515597.3:c.1984_1986del	XP_011513899.1:p.Ser662del
XM_011515598.1:c.1984_1986del	XP_011513900.1:p.Ser662del
XM_017012750.2:c.1984_1986del	XP_016868239.1:p.Ser662del
XM_017012751.2:c.1984_1986del	XP_016868240.1:p.Ser662del