Canonical Allele Identifier: CA367290302

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40041632T>C (hg19) ; chr7:g.40002033T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.40002033T>C , CM000669.2:g.40002033T>C	GRCh38
NC_000007.13:g.40041632T>C , CM000669.1:g.40041632T>C	GRCh37
NC_000007.12:g.40008157T>C	NCBI36
NG_052965.1:g.56674T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2353+2T>C MANE Select	ENSP00000181839.4:n.2353+2T>C
ENST00000340829.10:c.2353+2T>C	ENSP00000340557.5:n.2353+2T>C
ENST00000484589.2:c.905+2T>C
ENST00000642213.1:n.837T>C
ENST00000643859.1:c.1244+2T>C
ENST00000643915.1:c.667+2T>C	ENSP00000496187.1:n.667+2T>C
ENST00000645470.1:c.283+2T>C	ENSP00000495036.1:n.283+2T>C
ENST00000646039.1:c.1693+2T>C	ENSP00000494168.1:n.1693+2T>C
ENST00000647453.1:n.1422+2T>C
ENST00000181839.8:c.2353+2T>C	ENSP00000181839.4:n.2353+2T>C
ENST00000340829.9:c.2353+2T>C	ENSP00000340557.5:n.2353+2T>C
ENST00000484589.1:n.905+2T>C
ENST00000611390.1:c.511+2T>C	ENSP00000484610.1:n.511+2T>C
ENST00000613626.4:c.511+2T>C	ENSP00000480835.1:n.511+2T>C
NM_003718.4:c.2353+2T>C	NP_003709.3:n.2353+2T>C
NM_031267.3:c.2353+2T>C	NP_112557.2:n.2353+2T>C
XM_011515597.1:c.2353+2T>C	XP_011513899.1:n.2353+2T>C
XM_011515598.1:c.2353+2T>C	XP_011513900.1:n.2353+2T>C
XM_011515597.3:c.2353+2T>C	XP_011513899.1:n.2353+2T>C
XM_017012750.2:c.2353+2T>C	XP_016868239.1:n.2353+2T>C
XM_017012751.2:c.2353+2T>C	XP_016868240.1:n.2353+2T>C
NM_003718.5:c.2353+2T>C MANE Select	NP_003709.3:n.2353+2T>C