Canonical Allele Identifier: CA367309910

Gene: CDK13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39951162C>G , CM000669.2:g.39951162C>G	GRCh38
NC_000007.13:g.39990761C>G , CM000669.1:g.39990761C>G	GRCh37
NC_000007.12:g.39957286C>G	NCBI36
NG_052965.1:g.5803C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003718.5:c.521C>G MANE Select	NP_003709.3:p.Thr174Arg
ENST00000181839.10:c.521C>G MANE Select	ENSP00000181839.4:p.Thr174Arg
NM_003718.4:c.521C>G	NP_003709.3:p.Thr174Arg
NM_031267.3:c.521C>G	NP_112557.2:p.Thr174Arg
ENST00000181839.8:c.521C>G	ENSP00000181839.4:p.Thr174Arg
ENST00000340829.10:c.521C>G	ENSP00000340557.5:p.Thr174Arg
ENST00000340829.9:c.521C>G	ENSP00000340557.5:p.Thr174Arg
ENST00000613626.4:c.-1322C>G	ENSP00000480835.1:n.-1322C>G
ENST00000643868.1:c.145C>G
XM_011515597.1:c.521C>G	XP_011513899.1:p.Thr174Arg
XM_011515597.3:c.521C>G	XP_011513899.1:p.Thr174Arg
XM_011515598.1:c.521C>G	XP_011513900.1:p.Thr174Arg
XM_017012750.2:c.521C>G	XP_016868239.1:p.Thr174Arg
XM_017012751.2:c.521C>G	XP_016868240.1:p.Thr174Arg