Canonical Allele Identifier: CA454724028

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40039074T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999475T>G , CM000669.2:g.39999475T>G	GRCh38
NC_000007.13:g.40039074T>G , CM000669.1:g.40039074T>G	GRCh37
NC_000007.12:g.40005599T>G	NCBI36
NG_052965.1:g.54116T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000181839.10:c.2157T>G MANE Select	ENSP00000181839.4:p.Val719=
ENST00000340829.10:c.2157T>G	ENSP00000340557.5:p.Val719=
ENST00000484589.2:c.709T>G
ENST00000642213.1:n.639T>G
ENST00000643859.1:c.1048T>G
ENST00000643915.1:c.471T>G	ENSP00000496187.1:p.Val157=
ENST00000645470.1:c.87T>G	ENSP00000495036.1:p.Val29=
ENST00000646039.1:c.1497T>G	ENSP00000494168.1:p.Val499=
ENST00000647453.1:n.1226T>G
ENST00000647518.1:n.3994T>G
ENST00000181839.8:c.2157T>G	ENSP00000181839.4:p.Val719=
ENST00000340829.9:c.2157T>G	ENSP00000340557.5:p.Val719=
ENST00000484589.1:n.709T>G
ENST00000611390.1:c.315T>G	ENSP00000484610.1:p.Val105=
ENST00000613626.4:c.315T>G	ENSP00000480835.1:p.Val105=
NM_003718.4:c.2157T>G	NP_003709.3:p.Val719=
NM_031267.3:c.2157T>G	NP_112557.2:p.Val719=
XM_011515597.1:c.2157T>G	XP_011513899.1:p.Val719=
XM_011515598.1:c.2157T>G	XP_011513900.1:p.Val719=
XM_011515597.3:c.2157T>G	XP_011513899.1:p.Val719=
XM_017012750.2:c.2157T>G	XP_016868239.1:p.Val719=
XM_017012751.2:c.2157T>G	XP_016868240.1:p.Val719=
NM_003718.5:c.2157T>G MANE Select	NP_003709.3:p.Val719=