Canonical Allele Identifier: CA1701755712

Gene: CDK13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.40045921_40045922delinsCA , CM000669.2:g.40045921_40045922delinsCA	GRCh38
NC_000007.13:g.40085520_40085521delinsCA , CM000669.1:g.40085520_40085521delinsCA	GRCh37
NC_000007.12:g.40052045_40052046delinsCA	NCBI36
NG_052965.1:g.100562_100563delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000700485.1:n.175_176delinsCA
ENST00000700486.1:n.213_214delinsCA
ENST00000700487.1:n.181_182delinsCA
ENST00000181839.10:c.2439_2440delinsCA MANE Select	ENSP00000181839.4:p.His813=
ENST00000340829.10:c.2439_2440delinsCA	ENSP00000340557.5:p.His813=
ENST00000484589.2:c.991_992delinsCA
ENST00000643859.1:c.1330_1331delinsCA
ENST00000643915.1:c.753_754delinsCA	ENSP00000496187.1:p.His251=
ENST00000645470.1:c.369_370delinsCA	ENSP00000495036.1:p.His123=
ENST00000646039.1:c.1779_1780delinsCA	ENSP00000494168.1:p.His593=
ENST00000647453.1:n.1508_1509delinsCA
ENST00000181839.8:c.2439_2440delinsCA	ENSP00000181839.4:p.His813=
ENST00000340829.9:c.2439_2440delinsCA	ENSP00000340557.5:p.His813=
ENST00000484589.1:n.991_992delinsCA
ENST00000611390.1:c.597_598delinsCA	ENSP00000484610.1:p.His199=
ENST00000613626.4:c.597_598delinsCA	ENSP00000480835.1:p.His199=
NM_003718.4:c.2439_2440delinsCA	NP_003709.3:p.His813=
NM_031267.3:c.2439_2440delinsCA	NP_112557.2:p.His813=
XM_011515597.1:c.2439_2440delinsCA	XP_011513899.1:p.His813=
XM_011515598.1:c.2439_2440delinsCA	XP_011513900.1:p.His813=
XM_011515597.3:c.2439_2440delinsCA	XP_011513899.1:p.His813=
XM_017012750.2:c.2439_2440delinsCA	XP_016868239.1:p.His813=
XM_017012751.2:c.2439_2440delinsCA	XP_016868240.1:p.His813=
NM_003718.5:c.2439_2440delinsCA MANE Select	NP_003709.3:p.His813=