Canonical Allele Identifier: CA367288468

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40039082C>T (hg19) ; chr7:g.39999483C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999483C>T , CM000669.2:g.39999483C>T	GRCh38
NC_000007.13:g.40039082C>T , CM000669.1:g.40039082C>T	GRCh37
NC_000007.12:g.40005607C>T	NCBI36
NG_052965.1:g.54124C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2165C>T MANE Select	ENSP00000181839.4:p.Ala722Val
ENST00000340829.10:c.2165C>T	ENSP00000340557.5:p.Ala722Val
ENST00000484589.2:c.717C>T
ENST00000642213.1:n.647C>T
ENST00000643859.1:c.1056C>T
ENST00000643915.1:c.479C>T	ENSP00000496187.1:p.Ala160Val
ENST00000645470.1:c.95C>T	ENSP00000495036.1:p.Ala32Val
ENST00000646039.1:c.1505C>T	ENSP00000494168.1:p.Ala502Val
ENST00000647453.1:n.1234C>T
ENST00000647518.1:n.4002C>T
ENST00000181839.8:c.2165C>T	ENSP00000181839.4:p.Ala722Val
ENST00000340829.9:c.2165C>T	ENSP00000340557.5:p.Ala722Val
ENST00000484589.1:n.717C>T
ENST00000611390.1:c.323C>T	ENSP00000484610.1:p.Ala108Val
ENST00000613626.4:c.323C>T	ENSP00000480835.1:p.Ala108Val
NM_003718.4:c.2165C>T	NP_003709.3:p.Ala722Val
NM_031267.3:c.2165C>T	NP_112557.2:p.Ala722Val
XM_011515597.1:c.2165C>T	XP_011513899.1:p.Ala722Val
XM_011515598.1:c.2165C>T	XP_011513900.1:p.Ala722Val
XM_011515597.3:c.2165C>T	XP_011513899.1:p.Ala722Val
XM_017012750.2:c.2165C>T	XP_016868239.1:p.Ala722Val
XM_017012751.2:c.2165C>T	XP_016868240.1:p.Ala722Val
NM_003718.5:c.2165C>T MANE Select	NP_003709.3:p.Ala722Val