Canonical Allele Identifier: CA5113951

Gene: CDK20

Linked Data

• ClinVar Variation Id: 751435
• ClinVar RCV Id: RCV000928501
• dbSNP Id: rs780624824
• ExAC: 9:90582446 G / A
• gnomAD v2: 9-90582446-G-A
• gnomAD v3: 9-87967531-G-A
• gnomAD v4: 9-87967531-G-A
• MyVariant Identifiers: chr9:g.90582446G>A (hg19) ; chr9:g.87967531G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.87967531G>A , CM000671.2:g.87967531G>A	GRCh38
NC_000009.11:g.90582446G>A , CM000671.1:g.90582446G>A	GRCh37
NC_000009.10:g.89772266G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325303.9:c.972C>T MANE Select	ENSP00000322343.8:p.His324=
ENST00000325303.8:c.972C>T	ENSP00000322343.8:p.His324=
ENST00000336654.9:c.948C>T	ENSP00000338975.5:p.His316=
ENST00000375871.8:c.*53C>T	ENSP00000365031.3:n.*53C>T
ENST00000375883.7:c.909C>T	ENSP00000365043.3:p.His303=
ENST00000459720.5:n.2450C>T
ENST00000486228.7:n.1372C>T
ENST00000603475.1:n.4418C>T
ENST00000605159.5:c.*53C>T	ENSP00000474485.1:n.*53C>T
NM_001039803.2:c.972C>T	NP_001034892.1:p.His324=
NM_001170639.1:c.*53C>T	NP_001164110.1:n.*53C>T
NM_001170640.1:c.*53C>T	NP_001164111.1:n.*53C>T
NM_012119.4:c.909C>T	NP_036251.2:p.His303=
NM_178432.3:c.948C>T	NP_848519.1:p.His316=
XM_011518431.1:c.1026C>T	XP_011516733.1:p.His342=
XM_011518432.1:c.1011C>T	XP_011516734.1:p.His337=
XM_011518435.1:c.*53C>T	XP_011516737.1:n.*53C>T
XR_930090.1:n.89+309G>A
XM_017014561.2:c.987C>T	XP_016870050.1:p.His329=
XM_017014562.2:c.*76C>T	XP_016870051.1:n.*76C>T
XM_017014563.2:c.864C>T	XP_016870052.1:p.His288=
XM_017014564.2:c.*76C>T	XP_016870053.1:n.*76C>T
XR_001746263.2:n.1250C>T
XR_001746264.2:n.1256C>T
XR_001746265.2:n.1053C>T
NM_001170639.2:c.*53C>T	NP_001164110.1:n.*53C>T
NM_001039803.3:c.972C>T MANE Select	NP_001034892.1:p.His324=
NM_001170640.2:c.*53C>T	NP_001164111.1:n.*53C>T
NM_012119.5:c.909C>T	NP_036251.2:p.His303=
NM_178432.4:c.948C>T	NP_848519.1:p.His316=