Canonical Allele Identifier: CA367288290

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40039049T>C (hg19) ; chr7:g.39999450T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999450T>C , CM000669.2:g.39999450T>C	GRCh38
NC_000007.13:g.40039049T>C , CM000669.1:g.40039049T>C	GRCh37
NC_000007.12:g.40005574T>C	NCBI36
NG_052965.1:g.54091T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2132T>C MANE Select	ENSP00000181839.4:p.Ile711Thr
ENST00000340829.10:c.2132T>C	ENSP00000340557.5:p.Ile711Thr
ENST00000484589.2:c.684T>C
ENST00000642213.1:n.614T>C
ENST00000643859.1:c.1023T>C
ENST00000643915.1:c.446T>C	ENSP00000496187.1:p.Ile149Thr
ENST00000645470.1:c.62T>C	ENSP00000495036.1:p.Ile21Thr
ENST00000646039.1:c.1472T>C	ENSP00000494168.1:p.Ile491Thr
ENST00000646437.1:c.766T>C
ENST00000647453.1:n.1201T>C
ENST00000647518.1:n.3969T>C
ENST00000181839.8:c.2132T>C	ENSP00000181839.4:p.Ile711Thr
ENST00000340829.9:c.2132T>C	ENSP00000340557.5:p.Ile711Thr
ENST00000484589.1:n.684T>C
ENST00000611390.1:c.290T>C	ENSP00000484610.1:p.Ile97Thr
ENST00000613626.4:c.290T>C	ENSP00000480835.1:p.Ile97Thr
NM_003718.4:c.2132T>C	NP_003709.3:p.Ile711Thr
NM_031267.3:c.2132T>C	NP_112557.2:p.Ile711Thr
XM_011515597.1:c.2132T>C	XP_011513899.1:p.Ile711Thr
XM_011515598.1:c.2132T>C	XP_011513900.1:p.Ile711Thr
XM_011515597.3:c.2132T>C	XP_011513899.1:p.Ile711Thr
XM_017012750.2:c.2132T>C	XP_016868239.1:p.Ile711Thr
XM_017012751.2:c.2132T>C	XP_016868240.1:p.Ile711Thr
NM_003718.5:c.2132T>C MANE Select	NP_003709.3:p.Ile711Thr