Canonical Allele Identifier: CA454724011

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40039053A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999454A>C , CM000669.2:g.39999454A>C	GRCh38
NC_000007.13:g.40039053A>C , CM000669.1:g.40039053A>C	GRCh37
NC_000007.12:g.40005578A>C	NCBI36
NG_052965.1:g.54095A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2136A>C MANE Select	ENSP00000181839.4:p.Gly712=
ENST00000340829.10:c.2136A>C	ENSP00000340557.5:p.Gly712=
ENST00000484589.2:c.688A>C
ENST00000642213.1:n.618A>C
ENST00000643859.1:c.1027A>C
ENST00000643915.1:c.450A>C	ENSP00000496187.1:p.Gly150=
ENST00000645470.1:c.66A>C	ENSP00000495036.1:p.Gly22=
ENST00000646039.1:c.1476A>C	ENSP00000494168.1:p.Gly492=
ENST00000646437.1:c.770A>C
ENST00000647453.1:n.1205A>C
ENST00000647518.1:n.3973A>C
ENST00000181839.8:c.2136A>C	ENSP00000181839.4:p.Gly712=
ENST00000340829.9:c.2136A>C	ENSP00000340557.5:p.Gly712=
ENST00000484589.1:n.688A>C
ENST00000611390.1:c.294A>C	ENSP00000484610.1:p.Gly98=
ENST00000613626.4:c.294A>C	ENSP00000480835.1:p.Gly98=
NM_003718.4:c.2136A>C	NP_003709.3:p.Gly712=
NM_031267.3:c.2136A>C	NP_112557.2:p.Gly712=
XM_011515597.1:c.2136A>C	XP_011513899.1:p.Gly712=
XM_011515598.1:c.2136A>C	XP_011513900.1:p.Gly712=
XM_011515597.3:c.2136A>C	XP_011513899.1:p.Gly712=
XM_017012750.2:c.2136A>C	XP_016868239.1:p.Gly712=
XM_017012751.2:c.2136A>C	XP_016868240.1:p.Gly712=
NM_003718.5:c.2136A>C MANE Select	NP_003709.3:p.Gly712=