Canonical Allele Identifier: CA1701738238

Gene: CDK13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999381G= , CM000669.2:g.39999381G=	GRCh38
NC_000007.13:g.40038980G= , CM000669.1:g.40038980G=	GRCh37
NC_000007.12:g.40005505G=	NCBI36
NG_052965.1:g.54022G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2063G= MANE Select	ENSP00000181839.4:p.Gly688=
ENST00000340829.10:c.2063G=	ENSP00000340557.5:p.Gly688=
ENST00000484589.2:c.615G=
ENST00000642213.1:n.545G=
ENST00000642660.1:n.943G=
ENST00000643859.1:c.954G=
ENST00000643915.1:c.377G=	ENSP00000496187.1:p.Gly126=
ENST00000646039.1:c.1403G=	ENSP00000494168.1:p.Gly468=
ENST00000646437.1:c.697G=
ENST00000647453.1:n.1132G=
ENST00000647518.1:n.3900G=
ENST00000181839.8:c.2063G=	ENSP00000181839.4:p.Gly688=
ENST00000340829.9:c.2063G=	ENSP00000340557.5:p.Gly688=
ENST00000484589.1:n.615G=
ENST00000611390.1:c.221G=	ENSP00000484610.1:p.Gly74=
ENST00000613626.4:c.221G=	ENSP00000480835.1:p.Gly74=
NM_003718.4:c.2063G=	NP_003709.3:p.Gly688=
NM_031267.3:c.2063G=	NP_112557.2:p.Gly688=
XM_011515597.1:c.2063G=	XP_011513899.1:p.Gly688=
XM_011515598.1:c.2063G=	XP_011513900.1:p.Gly688=
XM_011515597.3:c.2063G=	XP_011513899.1:p.Gly688=
XM_017012750.2:c.2063G=	XP_016868239.1:p.Gly688=
XM_017012751.2:c.2063G=	XP_016868240.1:p.Gly688=
NM_003718.5:c.2063G= MANE Select	NP_003709.3:p.Gly688=