Canonical Allele Identifier: CA1701738297

Gene: CDK13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999528T= , CM000669.2:g.39999528T=	GRCh38
NC_000007.13:g.40039127T= , CM000669.1:g.40039127T=	GRCh37
NC_000007.12:g.40005652T=	NCBI36
NG_052965.1:g.54169T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2182+28T= MANE Select	ENSP00000181839.4:n.2182+28T=
ENST00000340829.10:c.2182+28T=	ENSP00000340557.5:n.2182+28T=
ENST00000484589.2:c.734+28T=
ENST00000642213.1:n.664+28T=
ENST00000643859.1:c.1073+28T=
ENST00000643915.1:c.496+28T=	ENSP00000496187.1:n.496+28T=
ENST00000645470.1:c.112+28T=	ENSP00000495036.1:n.112+28T=
ENST00000646039.1:c.1522+28T=	ENSP00000494168.1:n.1522+28T=
ENST00000647453.1:n.1251+28T=
ENST00000647518.1:n.4019+28T=
ENST00000181839.8:c.2182+28T=	ENSP00000181839.4:n.2182+28T=
ENST00000340829.9:c.2182+28T=	ENSP00000340557.5:n.2182+28T=
ENST00000484589.1:n.734+28T=
ENST00000611390.1:c.340+28T=	ENSP00000484610.1:n.340+28T=
ENST00000613626.4:c.340+28T=	ENSP00000480835.1:n.340+28T=
NM_003718.4:c.2182+28T=	NP_003709.3:n.2182+28T=
NM_031267.3:c.2182+28T=	NP_112557.2:n.2182+28T=
XM_011515597.1:c.2182+28T=	XP_011513899.1:n.2182+28T=
XM_011515598.1:c.2182+28T=	XP_011513900.1:n.2182+28T=
XM_011515597.3:c.2182+28T=	XP_011513899.1:n.2182+28T=
XM_017012750.2:c.2182+28T=	XP_016868239.1:n.2182+28T=
XM_017012751.2:c.2182+28T=	XP_016868240.1:n.2182+28T=
NM_003718.5:c.2182+28T= MANE Select	NP_003709.3:n.2182+28T=