Canonical Allele Identifier: CA1701738276

Gene: CDK13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999498C= , CM000669.2:g.39999498C=	GRCh38
NC_000007.13:g.40039097C= , CM000669.1:g.40039097C=	GRCh37
NC_000007.12:g.40005622C=	NCBI36
NG_052965.1:g.54139C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2180C= MANE Select	ENSP00000181839.4:p.Thr727=
ENST00000340829.10:c.2180C=	ENSP00000340557.5:p.Thr727=
ENST00000484589.2:c.732C=
ENST00000642213.1:n.662C=
ENST00000643859.1:c.1071C=
ENST00000643915.1:c.494C=	ENSP00000496187.1:p.Thr165=
ENST00000645470.1:c.110C=	ENSP00000495036.1:p.Thr37=
ENST00000646039.1:c.1520C=	ENSP00000494168.1:p.Thr507=
ENST00000647453.1:n.1249C=
ENST00000647518.1:n.4017C=
ENST00000181839.8:c.2180C=	ENSP00000181839.4:p.Thr727=
ENST00000340829.9:c.2180C=	ENSP00000340557.5:p.Thr727=
ENST00000484589.1:n.732C=
ENST00000611390.1:c.338C=	ENSP00000484610.1:p.Thr113=
ENST00000613626.4:c.338C=	ENSP00000480835.1:p.Thr113=
NM_003718.4:c.2180C=	NP_003709.3:p.Thr727=
NM_031267.3:c.2180C=	NP_112557.2:p.Thr727=
XM_011515597.1:c.2180C=	XP_011513899.1:p.Thr727=
XM_011515598.1:c.2180C=	XP_011513900.1:p.Thr727=
XM_011515597.3:c.2180C=	XP_011513899.1:p.Thr727=
XM_017012750.2:c.2180C=	XP_016868239.1:p.Thr727=
XM_017012751.2:c.2180C=	XP_016868240.1:p.Thr727=
NM_003718.5:c.2180C= MANE Select	NP_003709.3:p.Thr727=