Canonical Allele Identifier: CA367288100

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40039008G>C (hg19) ; chr7:g.39999409G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999409G>C , CM000669.2:g.39999409G>C	GRCh38
NC_000007.13:g.40039008G>C , CM000669.1:g.40039008G>C	GRCh37
NC_000007.12:g.40005533G>C	NCBI36
NG_052965.1:g.54050G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2091G>C MANE Select	ENSP00000181839.4:p.Trp697Cys
ENST00000340829.10:c.2091G>C	ENSP00000340557.5:p.Trp697Cys
ENST00000484589.2:c.643G>C
ENST00000642213.1:n.573G>C
ENST00000643859.1:c.982G>C
ENST00000643915.1:c.405G>C	ENSP00000496187.1:p.Trp135Cys
ENST00000645470.1:c.21G>C	ENSP00000495036.1:p.Trp7Cys
ENST00000646039.1:c.1431G>C	ENSP00000494168.1:p.Trp477Cys
ENST00000646437.1:c.725G>C
ENST00000647453.1:n.1160G>C
ENST00000647518.1:n.3928G>C
ENST00000181839.8:c.2091G>C	ENSP00000181839.4:p.Trp697Cys
ENST00000340829.9:c.2091G>C	ENSP00000340557.5:p.Trp697Cys
ENST00000484589.1:n.643G>C
ENST00000611390.1:c.249G>C	ENSP00000484610.1:p.Trp83Cys
ENST00000613626.4:c.249G>C	ENSP00000480835.1:p.Trp83Cys
NM_003718.4:c.2091G>C	NP_003709.3:p.Trp697Cys
NM_031267.3:c.2091G>C	NP_112557.2:p.Trp697Cys
XM_011515597.1:c.2091G>C	XP_011513899.1:p.Trp697Cys
XM_011515598.1:c.2091G>C	XP_011513900.1:p.Trp697Cys
XM_011515597.3:c.2091G>C	XP_011513899.1:p.Trp697Cys
XM_017012750.2:c.2091G>C	XP_016868239.1:p.Trp697Cys
XM_017012751.2:c.2091G>C	XP_016868240.1:p.Trp697Cys
NM_003718.5:c.2091G>C MANE Select	NP_003709.3:p.Trp697Cys