Canonical Allele Identifier: CA1701738262

Gene: CDK13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999443G= , CM000669.2:g.39999443G=	GRCh38
NC_000007.13:g.40039042G= , CM000669.1:g.40039042G=	GRCh37
NC_000007.12:g.40005567G=	NCBI36
NG_052965.1:g.54084G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2125G= MANE Select	ENSP00000181839.4:p.Gly709=
ENST00000340829.10:c.2125G=	ENSP00000340557.5:p.Gly709=
ENST00000484589.2:c.677G=
ENST00000642213.1:n.607G=
ENST00000643859.1:c.1016G=
ENST00000643915.1:c.439G=	ENSP00000496187.1:p.Gly147=
ENST00000645470.1:c.55G=	ENSP00000495036.1:p.Gly19=
ENST00000646039.1:c.1465G=	ENSP00000494168.1:p.Gly489=
ENST00000646437.1:c.759G=
ENST00000647453.1:n.1194G=
ENST00000647518.1:n.3962G=
ENST00000181839.8:c.2125G=	ENSP00000181839.4:p.Gly709=
ENST00000340829.9:c.2125G=	ENSP00000340557.5:p.Gly709=
ENST00000484589.1:n.677G=
ENST00000611390.1:c.283G=	ENSP00000484610.1:p.Gly95=
ENST00000613626.4:c.283G=	ENSP00000480835.1:p.Gly95=
NM_003718.4:c.2125G=	NP_003709.3:p.Gly709=
NM_031267.3:c.2125G=	NP_112557.2:p.Gly709=
XM_011515597.1:c.2125G=	XP_011513899.1:p.Gly709=
XM_011515598.1:c.2125G=	XP_011513900.1:p.Gly709=
XM_011515597.3:c.2125G=	XP_011513899.1:p.Gly709=
XM_017012750.2:c.2125G=	XP_016868239.1:p.Gly709=
XM_017012751.2:c.2125G=	XP_016868240.1:p.Gly709=
NM_003718.5:c.2125G= MANE Select	NP_003709.3:p.Gly709=