Canonical Allele Identifier: CA454723963

Gene: CDK13

Linked Data

• ClinVar Variation Id: 2762892
• ClinVar RCV Id: RCV003570315
• gnomAD v4: 7-39999370-G-A
• MyVariant Identifiers: chr7:g.40038969G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999370G>A , CM000669.2:g.39999370G>A	GRCh38
NC_000007.13:g.40038969G>A , CM000669.1:g.40038969G>A	GRCh37
NC_000007.12:g.40005494G>A	NCBI36
NG_052965.1:g.54011G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000181839.10:c.2052G>A MANE Select	ENSP00000181839.4:p.Gly684=
ENST00000340829.10:c.2052G>A	ENSP00000340557.5:p.Gly684=
ENST00000484589.2:c.604G>A
ENST00000642213.1:n.534G>A
ENST00000642660.1:n.932G>A
ENST00000643859.1:c.943G>A
ENST00000643915.1:c.366G>A	ENSP00000496187.1:p.Gly122=
ENST00000646039.1:c.1392G>A	ENSP00000494168.1:p.Gly464=
ENST00000646437.1:c.686G>A
ENST00000647453.1:n.1121G>A
ENST00000647518.1:n.3889G>A
ENST00000181839.8:c.2052G>A	ENSP00000181839.4:p.Gly684=
ENST00000340829.9:c.2052G>A	ENSP00000340557.5:p.Gly684=
ENST00000484589.1:n.604G>A
ENST00000611390.1:c.210G>A	ENSP00000484610.1:p.Gly70=
ENST00000613626.4:c.210G>A	ENSP00000480835.1:p.Gly70=
NM_003718.4:c.2052G>A	NP_003709.3:p.Gly684=
NM_031267.3:c.2052G>A	NP_112557.2:p.Gly684=
XM_011515597.1:c.2052G>A	XP_011513899.1:p.Gly684=
XM_011515598.1:c.2052G>A	XP_011513900.1:p.Gly684=
XM_011515597.3:c.2052G>A	XP_011513899.1:p.Gly684=
XM_017012750.2:c.2052G>A	XP_016868239.1:p.Gly684=
XM_017012751.2:c.2052G>A	XP_016868240.1:p.Gly684=
NM_003718.5:c.2052G>A MANE Select	NP_003709.3:p.Gly684=