Canonical Allele Identifier: CA367288206

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40039031T>G (hg19) ; chr7:g.39999432T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999432T>G , CM000669.2:g.39999432T>G	GRCh38
NC_000007.13:g.40039031T>G , CM000669.1:g.40039031T>G	GRCh37
NC_000007.12:g.40005556T>G	NCBI36
NG_052965.1:g.54073T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2114T>G MANE Select	ENSP00000181839.4:p.Phe705Cys
ENST00000340829.10:c.2114T>G	ENSP00000340557.5:p.Phe705Cys
ENST00000484589.2:c.666T>G
ENST00000642213.1:n.596T>G
ENST00000643859.1:c.1005T>G
ENST00000643915.1:c.428T>G	ENSP00000496187.1:p.Phe143Cys
ENST00000645470.1:c.44T>G	ENSP00000495036.1:p.Phe15Cys
ENST00000646039.1:c.1454T>G	ENSP00000494168.1:p.Phe485Cys
ENST00000646437.1:c.748T>G
ENST00000647453.1:n.1183T>G
ENST00000647518.1:n.3951T>G
ENST00000181839.8:c.2114T>G	ENSP00000181839.4:p.Phe705Cys
ENST00000340829.9:c.2114T>G	ENSP00000340557.5:p.Phe705Cys
ENST00000484589.1:n.666T>G
ENST00000611390.1:c.272T>G	ENSP00000484610.1:p.Phe91Cys
ENST00000613626.4:c.272T>G	ENSP00000480835.1:p.Phe91Cys
NM_003718.4:c.2114T>G	NP_003709.3:p.Phe705Cys
NM_031267.3:c.2114T>G	NP_112557.2:p.Phe705Cys
XM_011515597.1:c.2114T>G	XP_011513899.1:p.Phe705Cys
XM_011515598.1:c.2114T>G	XP_011513900.1:p.Phe705Cys
XM_011515597.3:c.2114T>G	XP_011513899.1:p.Phe705Cys
XM_017012750.2:c.2114T>G	XP_016868239.1:p.Phe705Cys
XM_017012751.2:c.2114T>G	XP_016868240.1:p.Phe705Cys
NM_003718.5:c.2114T>G MANE Select	NP_003709.3:p.Phe705Cys