Canonical Allele Identifier: CA454723485

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40085616A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.40046017A>T , CM000669.2:g.40046017A>T	GRCh38
NC_000007.13:g.40085616A>T , CM000669.1:g.40085616A>T	GRCh37
NC_000007.12:g.40052141A>T	NCBI36
NG_052965.1:g.100658A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000700485.1:n.271A>T
ENST00000700486.1:n.309A>T
ENST00000700487.1:n.277A>T
ENST00000181839.10:c.2535A>T MANE Select	ENSP00000181839.4:p.Leu845=
ENST00000340829.10:c.2535A>T	ENSP00000340557.5:p.Leu845=
ENST00000484589.2:c.1087A>T
ENST00000642592.1:c.88A>T
ENST00000643859.1:c.1426A>T
ENST00000643915.1:c.849A>T	ENSP00000496187.1:p.Leu283=
ENST00000645470.1:c.465A>T	ENSP00000495036.1:p.Leu155=
ENST00000646039.1:c.1875A>T	ENSP00000494168.1:p.Leu625=
ENST00000647453.1:n.1604A>T
ENST00000181839.8:c.2535A>T	ENSP00000181839.4:p.Leu845=
ENST00000340829.9:c.2535A>T	ENSP00000340557.5:p.Leu845=
ENST00000484589.1:n.1087A>T
ENST00000611390.1:c.693A>T	ENSP00000484610.1:p.Leu231=
ENST00000613626.4:c.693A>T	ENSP00000480835.1:p.Leu231=
NM_003718.4:c.2535A>T	NP_003709.3:p.Leu845=
NM_031267.3:c.2535A>T	NP_112557.2:p.Leu845=
XM_011515597.1:c.2535A>T	XP_011513899.1:p.Leu845=
XM_011515598.1:c.2535A>T	XP_011513900.1:p.Leu845=
XM_011515597.3:c.2535A>T	XP_011513899.1:p.Leu845=
XM_017012750.2:c.2535A>T	XP_016868239.1:p.Leu845=
XM_017012751.2:c.2535A>T	XP_016868240.1:p.Leu845=
NM_003718.5:c.2535A>T MANE Select	NP_003709.3:p.Leu845=