Canonical Allele Identifier: CA367288137

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40039019G>A (hg19) ; chr7:g.39999420G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999420G>A , CM000669.2:g.39999420G>A	GRCh38
NC_000007.13:g.40039019G>A , CM000669.1:g.40039019G>A	GRCh37
NC_000007.12:g.40005544G>A	NCBI36
NG_052965.1:g.54061G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2102G>A MANE Select	ENSP00000181839.4:p.Cys701Tyr
ENST00000340829.10:c.2102G>A	ENSP00000340557.5:p.Cys701Tyr
ENST00000484589.2:c.654G>A
ENST00000642213.1:n.584G>A
ENST00000643859.1:c.993G>A
ENST00000643915.1:c.416G>A	ENSP00000496187.1:p.Cys139Tyr
ENST00000645470.1:c.32G>A	ENSP00000495036.1:p.Cys11Tyr
ENST00000646039.1:c.1442G>A	ENSP00000494168.1:p.Cys481Tyr
ENST00000646437.1:c.736G>A
ENST00000647453.1:n.1171G>A
ENST00000647518.1:n.3939G>A
ENST00000181839.8:c.2102G>A	ENSP00000181839.4:p.Cys701Tyr
ENST00000340829.9:c.2102G>A	ENSP00000340557.5:p.Cys701Tyr
ENST00000484589.1:n.654G>A
ENST00000611390.1:c.260G>A	ENSP00000484610.1:p.Cys87Tyr
ENST00000613626.4:c.260G>A	ENSP00000480835.1:p.Cys87Tyr
NM_003718.4:c.2102G>A	NP_003709.3:p.Cys701Tyr
NM_031267.3:c.2102G>A	NP_112557.2:p.Cys701Tyr
XM_011515597.1:c.2102G>A	XP_011513899.1:p.Cys701Tyr
XM_011515598.1:c.2102G>A	XP_011513900.1:p.Cys701Tyr
XM_011515597.3:c.2102G>A	XP_011513899.1:p.Cys701Tyr
XM_017012750.2:c.2102G>A	XP_016868239.1:p.Cys701Tyr
XM_017012751.2:c.2102G>A	XP_016868240.1:p.Cys701Tyr
NM_003718.5:c.2102G>A MANE Select	NP_003709.3:p.Cys701Tyr