Canonical Allele Identifier: CA367279829

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40085507T>A (hg19) ; chr7:g.40045908T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.40045908T>A , CM000669.2:g.40045908T>A	GRCh38
NC_000007.13:g.40085507T>A , CM000669.1:g.40085507T>A	GRCh37
NC_000007.12:g.40052032T>A	NCBI36
NG_052965.1:g.100549T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700485.1:n.162T>A
ENST00000700486.1:n.200T>A
ENST00000700487.1:n.168T>A
ENST00000181839.10:c.2426T>A MANE Select	ENSP00000181839.4:p.Phe809Tyr
ENST00000340829.10:c.2426T>A	ENSP00000340557.5:p.Phe809Tyr
ENST00000484589.2:c.978T>A
ENST00000643859.1:c.1317T>A
ENST00000643915.1:c.740T>A	ENSP00000496187.1:p.Phe247Tyr
ENST00000645470.1:c.356T>A	ENSP00000495036.1:p.Phe119Tyr
ENST00000646039.1:c.1766T>A	ENSP00000494168.1:p.Phe589Tyr
ENST00000647453.1:n.1495T>A
ENST00000181839.8:c.2426T>A	ENSP00000181839.4:p.Phe809Tyr
ENST00000340829.9:c.2426T>A	ENSP00000340557.5:p.Phe809Tyr
ENST00000484589.1:n.978T>A
ENST00000611390.1:c.584T>A	ENSP00000484610.1:p.Phe195Tyr
ENST00000613626.4:c.584T>A	ENSP00000480835.1:p.Phe195Tyr
NM_003718.4:c.2426T>A	NP_003709.3:p.Phe809Tyr
NM_031267.3:c.2426T>A	NP_112557.2:p.Phe809Tyr
XM_011515597.1:c.2426T>A	XP_011513899.1:p.Phe809Tyr
XM_011515598.1:c.2426T>A	XP_011513900.1:p.Phe809Tyr
XM_011515597.3:c.2426T>A	XP_011513899.1:p.Phe809Tyr
XM_017012750.2:c.2426T>A	XP_016868239.1:p.Phe809Tyr
XM_017012751.2:c.2426T>A	XP_016868240.1:p.Phe809Tyr
NM_003718.5:c.2426T>A MANE Select	NP_003709.3:p.Phe809Tyr