Canonical Allele Identifier: CA454724010

Gene: CDK13

Linked Data

• dbSNP Id: rs1583969400
• MyVariant Identifiers: chr7:g.40039050T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999451T>C , CM000669.2:g.39999451T>C	GRCh38
NC_000007.13:g.40039050T>C , CM000669.1:g.40039050T>C	GRCh37
NC_000007.12:g.40005575T>C	NCBI36
NG_052965.1:g.54092T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2133T>C MANE Select	ENSP00000181839.4:p.Ile711=
ENST00000340829.10:c.2133T>C	ENSP00000340557.5:p.Ile711=
ENST00000484589.2:c.685T>C
ENST00000642213.1:n.615T>C
ENST00000643859.1:c.1024T>C
ENST00000643915.1:c.447T>C	ENSP00000496187.1:p.Ile149=
ENST00000645470.1:c.63T>C	ENSP00000495036.1:p.Ile21=
ENST00000646039.1:c.1473T>C	ENSP00000494168.1:p.Ile491=
ENST00000646437.1:c.767T>C
ENST00000647453.1:n.1202T>C
ENST00000647518.1:n.3970T>C
ENST00000181839.8:c.2133T>C	ENSP00000181839.4:p.Ile711=
ENST00000340829.9:c.2133T>C	ENSP00000340557.5:p.Ile711=
ENST00000484589.1:n.685T>C
ENST00000611390.1:c.291T>C	ENSP00000484610.1:p.Ile97=
ENST00000613626.4:c.291T>C	ENSP00000480835.1:p.Ile97=
NM_003718.4:c.2133T>C	NP_003709.3:p.Ile711=
NM_031267.3:c.2133T>C	NP_112557.2:p.Ile711=
XM_011515597.1:c.2133T>C	XP_011513899.1:p.Ile711=
XM_011515598.1:c.2133T>C	XP_011513900.1:p.Ile711=
XM_011515597.3:c.2133T>C	XP_011513899.1:p.Ile711=
XM_017012750.2:c.2133T>C	XP_016868239.1:p.Ile711=
XM_017012751.2:c.2133T>C	XP_016868240.1:p.Ile711=
NM_003718.5:c.2133T>C MANE Select	NP_003709.3:p.Ile711=