Canonical Allele Identifier: CA454723430

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40085508T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.40045909T>C , CM000669.2:g.40045909T>C	GRCh38
NC_000007.13:g.40085508T>C , CM000669.1:g.40085508T>C	GRCh37
NC_000007.12:g.40052033T>C	NCBI36
NG_052965.1:g.100550T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700485.1:n.163T>C
ENST00000700486.1:n.201T>C
ENST00000700487.1:n.169T>C
ENST00000181839.10:c.2427T>C MANE Select	ENSP00000181839.4:p.Phe809=
ENST00000340829.10:c.2427T>C	ENSP00000340557.5:p.Phe809=
ENST00000484589.2:c.979T>C
ENST00000643859.1:c.1318T>C
ENST00000643915.1:c.741T>C	ENSP00000496187.1:p.Phe247=
ENST00000645470.1:c.357T>C	ENSP00000495036.1:p.Phe119=
ENST00000646039.1:c.1767T>C	ENSP00000494168.1:p.Phe589=
ENST00000647453.1:n.1496T>C
ENST00000181839.8:c.2427T>C	ENSP00000181839.4:p.Phe809=
ENST00000340829.9:c.2427T>C	ENSP00000340557.5:p.Phe809=
ENST00000484589.1:n.979T>C
ENST00000611390.1:c.585T>C	ENSP00000484610.1:p.Phe195=
ENST00000613626.4:c.585T>C	ENSP00000480835.1:p.Phe195=
NM_003718.4:c.2427T>C	NP_003709.3:p.Phe809=
NM_031267.3:c.2427T>C	NP_112557.2:p.Phe809=
XM_011515597.1:c.2427T>C	XP_011513899.1:p.Phe809=
XM_011515598.1:c.2427T>C	XP_011513900.1:p.Phe809=
XM_011515597.3:c.2427T>C	XP_011513899.1:p.Phe809=
XM_017012750.2:c.2427T>C	XP_016868239.1:p.Phe809=
XM_017012751.2:c.2427T>C	XP_016868240.1:p.Phe809=
NM_003718.5:c.2427T>C MANE Select	NP_003709.3:p.Phe809=