Canonical Allele Identifier: CA454724035

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40039084A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999485A>C , CM000669.2:g.39999485A>C	GRCh38
NC_000007.13:g.40039084A>C , CM000669.1:g.40039084A>C	GRCh37
NC_000007.12:g.40005609A>C	NCBI36
NG_052965.1:g.54126A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2167A>C MANE Select	ENSP00000181839.4:p.Arg723=
ENST00000340829.10:c.2167A>C	ENSP00000340557.5:p.Arg723=
ENST00000484589.2:c.719A>C
ENST00000642213.1:n.649A>C
ENST00000643859.1:c.1058A>C
ENST00000643915.1:c.481A>C	ENSP00000496187.1:p.Arg161=
ENST00000645470.1:c.97A>C	ENSP00000495036.1:p.Arg33=
ENST00000646039.1:c.1507A>C	ENSP00000494168.1:p.Arg503=
ENST00000647453.1:n.1236A>C
ENST00000647518.1:n.4004A>C
ENST00000181839.8:c.2167A>C	ENSP00000181839.4:p.Arg723=
ENST00000340829.9:c.2167A>C	ENSP00000340557.5:p.Arg723=
ENST00000484589.1:n.719A>C
ENST00000611390.1:c.325A>C	ENSP00000484610.1:p.Arg109=
ENST00000613626.4:c.325A>C	ENSP00000480835.1:p.Arg109=
NM_003718.4:c.2167A>C	NP_003709.3:p.Arg723=
NM_031267.3:c.2167A>C	NP_112557.2:p.Arg723=
XM_011515597.1:c.2167A>C	XP_011513899.1:p.Arg723=
XM_011515598.1:c.2167A>C	XP_011513900.1:p.Arg723=
XM_011515597.3:c.2167A>C	XP_011513899.1:p.Arg723=
XM_017012750.2:c.2167A>C	XP_016868239.1:p.Arg723=
XM_017012751.2:c.2167A>C	XP_016868240.1:p.Arg723=
NM_003718.5:c.2167A>C MANE Select	NP_003709.3:p.Arg723=