Canonical Allele Identifier: CA367288414

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40039072G>T (hg19) ; chr7:g.39999473G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999473G>T , CM000669.2:g.39999473G>T	GRCh38
NC_000007.13:g.40039072G>T , CM000669.1:g.40039072G>T	GRCh37
NC_000007.12:g.40005597G>T	NCBI36
NG_052965.1:g.54114G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000181839.10:c.2155G>T MANE Select	ENSP00000181839.4:p.Val719Phe
ENST00000340829.10:c.2155G>T	ENSP00000340557.5:p.Val719Phe
ENST00000484589.2:c.707G>T
ENST00000642213.1:n.637G>T
ENST00000643859.1:c.1046G>T
ENST00000643915.1:c.469G>T	ENSP00000496187.1:p.Val157Phe
ENST00000645470.1:c.85G>T	ENSP00000495036.1:p.Val29Phe
ENST00000646039.1:c.1495G>T	ENSP00000494168.1:p.Val499Phe
ENST00000647453.1:n.1224G>T
ENST00000647518.1:n.3992G>T
ENST00000181839.8:c.2155G>T	ENSP00000181839.4:p.Val719Phe
ENST00000340829.9:c.2155G>T	ENSP00000340557.5:p.Val719Phe
ENST00000484589.1:n.707G>T
ENST00000611390.1:c.313G>T	ENSP00000484610.1:p.Val105Phe
ENST00000613626.4:c.313G>T	ENSP00000480835.1:p.Val105Phe
NM_003718.4:c.2155G>T	NP_003709.3:p.Val719Phe
NM_031267.3:c.2155G>T	NP_112557.2:p.Val719Phe
XM_011515597.1:c.2155G>T	XP_011513899.1:p.Val719Phe
XM_011515598.1:c.2155G>T	XP_011513900.1:p.Val719Phe
XM_011515597.3:c.2155G>T	XP_011513899.1:p.Val719Phe
XM_017012750.2:c.2155G>T	XP_016868239.1:p.Val719Phe
XM_017012751.2:c.2155G>T	XP_016868240.1:p.Val719Phe
NM_003718.5:c.2155G>T MANE Select	NP_003709.3:p.Val719Phe