Canonical Allele Identifier: CA367280244

Gene: CDK13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.40045989G>T , CM000669.2:g.40045989G>T	GRCh38
NC_000007.13:g.40085588G>T , CM000669.1:g.40085588G>T	GRCh37
NC_000007.12:g.40052113G>T	NCBI36
NG_052965.1:g.100630G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003718.5:c.2507G>T MANE Select	NP_003709.3:p.Arg836Ile
ENST00000181839.10:c.2507G>T MANE Select	ENSP00000181839.4:p.Arg836Ile
NM_003718.4:c.2507G>T	NP_003709.3:p.Arg836Ile
NM_031267.3:c.2507G>T	NP_112557.2:p.Arg836Ile
ENST00000181839.8:c.2507G>T	ENSP00000181839.4:p.Arg836Ile
ENST00000340829.10:c.2507G>T	ENSP00000340557.5:p.Arg836Ile
ENST00000340829.9:c.2507G>T	ENSP00000340557.5:p.Arg836Ile
ENST00000484589.1:n.1059G>T
ENST00000484589.2:c.1059G>T
ENST00000611390.1:c.665G>T	ENSP00000484610.1:p.Arg222Ile
ENST00000613626.4:c.665G>T	ENSP00000480835.1:p.Arg222Ile
ENST00000642592.1:c.60G>T
ENST00000643859.1:c.1398G>T
ENST00000643915.1:c.821G>T	ENSP00000496187.1:p.Arg274Ile
ENST00000645470.1:c.437G>T	ENSP00000495036.1:p.Arg146Ile
ENST00000646039.1:c.1847G>T	ENSP00000494168.1:p.Arg616Ile
ENST00000647453.1:n.1576G>T
ENST00000700485.1:n.243G>T
ENST00000700486.1:n.281G>T
ENST00000700487.1:n.249G>T
XM_011515597.1:c.2507G>T	XP_011513899.1:p.Arg836Ile
XM_011515597.3:c.2507G>T	XP_011513899.1:p.Arg836Ile
XM_011515598.1:c.2507G>T	XP_011513900.1:p.Arg836Ile
XM_017012750.2:c.2507G>T	XP_016868239.1:p.Arg836Ile
XM_017012751.2:c.2507G>T	XP_016868240.1:p.Arg836Ile