Canonical Allele Identifier: CA367288324

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40039055A>T (hg19) ; chr7:g.39999456A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999456A>T , CM000669.2:g.39999456A>T	GRCh38
NC_000007.13:g.40039055A>T , CM000669.1:g.40039055A>T	GRCh37
NC_000007.12:g.40005580A>T	NCBI36
NG_052965.1:g.54097A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000181839.10:c.2138A>T MANE Select	ENSP00000181839.4:p.Glu713Val
ENST00000340829.10:c.2138A>T	ENSP00000340557.5:p.Glu713Val
ENST00000484589.2:c.690A>T
ENST00000642213.1:n.620A>T
ENST00000643859.1:c.1029A>T
ENST00000643915.1:c.452A>T	ENSP00000496187.1:p.Glu151Val
ENST00000645470.1:c.68A>T	ENSP00000495036.1:p.Glu23Val
ENST00000646039.1:c.1478A>T	ENSP00000494168.1:p.Glu493Val
ENST00000646437.1:c.772A>T
ENST00000647453.1:n.1207A>T
ENST00000647518.1:n.3975A>T
ENST00000181839.8:c.2138A>T	ENSP00000181839.4:p.Glu713Val
ENST00000340829.9:c.2138A>T	ENSP00000340557.5:p.Glu713Val
ENST00000484589.1:n.690A>T
ENST00000611390.1:c.296A>T	ENSP00000484610.1:p.Glu99Val
ENST00000613626.4:c.296A>T	ENSP00000480835.1:p.Glu99Val
NM_003718.4:c.2138A>T	NP_003709.3:p.Glu713Val
NM_031267.3:c.2138A>T	NP_112557.2:p.Glu713Val
XM_011515597.1:c.2138A>T	XP_011513899.1:p.Glu713Val
XM_011515598.1:c.2138A>T	XP_011513900.1:p.Glu713Val
XM_011515597.3:c.2138A>T	XP_011513899.1:p.Glu713Val
XM_017012750.2:c.2138A>T	XP_016868239.1:p.Glu713Val
XM_017012751.2:c.2138A>T	XP_016868240.1:p.Glu713Val
NM_003718.5:c.2138A>T MANE Select	NP_003709.3:p.Glu713Val