Canonical Allele Identifier: CA454724008

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40039047T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999448T>C , CM000669.2:g.39999448T>C	GRCh38
NC_000007.13:g.40039047T>C , CM000669.1:g.40039047T>C	GRCh37
NC_000007.12:g.40005572T>C	NCBI36
NG_052965.1:g.54089T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2130T>C MANE Select	ENSP00000181839.4:p.Ile710=
ENST00000340829.10:c.2130T>C	ENSP00000340557.5:p.Ile710=
ENST00000484589.2:c.682T>C
ENST00000642213.1:n.612T>C
ENST00000643859.1:c.1021T>C
ENST00000643915.1:c.444T>C	ENSP00000496187.1:p.Ile148=
ENST00000645470.1:c.60T>C	ENSP00000495036.1:p.Ile20=
ENST00000646039.1:c.1470T>C	ENSP00000494168.1:p.Ile490=
ENST00000646437.1:c.764T>C
ENST00000647453.1:n.1199T>C
ENST00000647518.1:n.3967T>C
ENST00000181839.8:c.2130T>C	ENSP00000181839.4:p.Ile710=
ENST00000340829.9:c.2130T>C	ENSP00000340557.5:p.Ile710=
ENST00000484589.1:n.682T>C
ENST00000611390.1:c.288T>C	ENSP00000484610.1:p.Ile96=
ENST00000613626.4:c.288T>C	ENSP00000480835.1:p.Ile96=
NM_003718.4:c.2130T>C	NP_003709.3:p.Ile710=
NM_031267.3:c.2130T>C	NP_112557.2:p.Ile710=
XM_011515597.1:c.2130T>C	XP_011513899.1:p.Ile710=
XM_011515598.1:c.2130T>C	XP_011513900.1:p.Ile710=
XM_011515597.3:c.2130T>C	XP_011513899.1:p.Ile710=
XM_017012750.2:c.2130T>C	XP_016868239.1:p.Ile710=
XM_017012751.2:c.2130T>C	XP_016868240.1:p.Ile710=
NM_003718.5:c.2130T>C MANE Select	NP_003709.3:p.Ile710=