Canonical Allele Identifier: CA367290091

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40041602A>C (hg19) ; chr7:g.40002003A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.40002003A>C , CM000669.2:g.40002003A>C	GRCh38
NC_000007.13:g.40041602A>C , CM000669.1:g.40041602A>C	GRCh37
NC_000007.12:g.40008127A>C	NCBI36
NG_052965.1:g.56644A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2325A>C MANE Select	ENSP00000181839.4:p.Glu775Asp
ENST00000340829.10:c.2325A>C	ENSP00000340557.5:p.Glu775Asp
ENST00000484589.2:c.877A>C
ENST00000642213.1:n.807A>C
ENST00000643859.1:c.1216A>C
ENST00000643915.1:c.639A>C	ENSP00000496187.1:p.Glu213Asp
ENST00000645470.1:c.255A>C	ENSP00000495036.1:p.Glu85Asp
ENST00000646039.1:c.1665A>C	ENSP00000494168.1:p.Glu555Asp
ENST00000647453.1:n.1394A>C
ENST00000647518.1:n.4162A>C
ENST00000181839.8:c.2325A>C	ENSP00000181839.4:p.Glu775Asp
ENST00000340829.9:c.2325A>C	ENSP00000340557.5:p.Glu775Asp
ENST00000484589.1:n.877A>C
ENST00000611390.1:c.483A>C	ENSP00000484610.1:p.Glu161Asp
ENST00000613626.4:c.483A>C	ENSP00000480835.1:p.Glu161Asp
NM_003718.4:c.2325A>C	NP_003709.3:p.Glu775Asp
NM_031267.3:c.2325A>C	NP_112557.2:p.Glu775Asp
XM_011515597.1:c.2325A>C	XP_011513899.1:p.Glu775Asp
XM_011515598.1:c.2325A>C	XP_011513900.1:p.Glu775Asp
XM_011515597.3:c.2325A>C	XP_011513899.1:p.Glu775Asp
XM_017012750.2:c.2325A>C	XP_016868239.1:p.Glu775Asp
XM_017012751.2:c.2325A>C	XP_016868240.1:p.Glu775Asp
NM_003718.5:c.2325A>C MANE Select	NP_003709.3:p.Glu775Asp