Canonical Allele Identifier: CA367279845

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40085513A>T (hg19) ; chr7:g.40045914A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.40045914A>T , CM000669.2:g.40045914A>T	GRCh38
NC_000007.13:g.40085513A>T , CM000669.1:g.40085513A>T	GRCh37
NC_000007.12:g.40052038A>T	NCBI36
NG_052965.1:g.100555A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700485.1:n.168A>T
ENST00000700486.1:n.206A>T
ENST00000700487.1:n.174A>T
ENST00000181839.10:c.2432A>T MANE Select	ENSP00000181839.4:p.Glu811Val
ENST00000340829.10:c.2432A>T	ENSP00000340557.5:p.Glu811Val
ENST00000484589.2:c.984A>T
ENST00000643859.1:c.1323A>T
ENST00000643915.1:c.746A>T	ENSP00000496187.1:p.Glu249Val
ENST00000645470.1:c.362A>T	ENSP00000495036.1:p.Glu121Val
ENST00000646039.1:c.1772A>T	ENSP00000494168.1:p.Glu591Val
ENST00000647453.1:n.1501A>T
ENST00000181839.8:c.2432A>T	ENSP00000181839.4:p.Glu811Val
ENST00000340829.9:c.2432A>T	ENSP00000340557.5:p.Glu811Val
ENST00000484589.1:n.984A>T
ENST00000611390.1:c.590A>T	ENSP00000484610.1:p.Glu197Val
ENST00000613626.4:c.590A>T	ENSP00000480835.1:p.Glu197Val
NM_003718.4:c.2432A>T	NP_003709.3:p.Glu811Val
NM_031267.3:c.2432A>T	NP_112557.2:p.Glu811Val
XM_011515597.1:c.2432A>T	XP_011513899.1:p.Glu811Val
XM_011515598.1:c.2432A>T	XP_011513900.1:p.Glu811Val
XM_011515597.3:c.2432A>T	XP_011513899.1:p.Glu811Val
XM_017012750.2:c.2432A>T	XP_016868239.1:p.Glu811Val
XM_017012751.2:c.2432A>T	XP_016868240.1:p.Glu811Val
NM_003718.5:c.2432A>T MANE Select	NP_003709.3:p.Glu811Val