Canonical Allele Identifier: CA373978284

Gene: CDK20

Linked Data

• MyVariant Identifiers: chr9:g.90584786G>T (hg19) ; chr9:g.87969871G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.87969871G>T , CM000671.2:g.87969871G>T	GRCh38
NC_000009.11:g.90584786G>T , CM000671.1:g.90584786G>T	GRCh37
NC_000009.10:g.89774606G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325303.9:c.612C>A MANE Select	ENSP00000322343.8:p.Phe204Leu
ENST00000325303.8:c.612C>A	ENSP00000322343.8:p.Phe204Leu
ENST00000336654.9:c.588C>A	ENSP00000338975.5:p.Phe196Leu
ENST00000375871.8:c.501-522C>A	ENSP00000365031.3:n.501-522C>A
ENST00000375883.7:c.549C>A	ENSP00000365043.3:p.Phe183Leu
ENST00000459720.5:n.1644C>A
ENST00000486228.7:n.1012C>A
ENST00000603475.1:n.2078C>A
ENST00000605159.5:c.549C>A	ENSP00000474485.1:p.Phe183Leu
NM_001039803.2:c.612C>A	NP_001034892.1:p.Phe204Leu
NM_001170639.1:c.549C>A	NP_001164110.1:p.Phe183Leu
NM_001170640.1:c.501-522C>A	NP_001164111.1:n.501-522C>A
NM_012119.4:c.549C>A	NP_036251.2:p.Phe183Leu
NM_178432.3:c.588C>A	NP_848519.1:p.Phe196Leu
XM_011518425.1:c.666C>A	XP_011516727.1:p.Phe222Leu
XM_011518426.1:c.651C>A	XP_011516728.1:p.Phe217Leu
XM_011518427.1:c.627C>A	XP_011516729.1:p.Phe209Leu
XM_011518428.1:c.612C>A	XP_011516730.1:p.Phe204Leu
XM_011518429.1:c.588C>A	XP_011516731.1:p.Phe196Leu
XM_011518430.1:c.549C>A	XP_011516732.1:p.Phe183Leu
XM_011518431.1:c.666C>A	XP_011516733.1:p.Phe222Leu
XM_011518432.1:c.651C>A	XP_011516734.1:p.Phe217Leu
XM_011518433.1:c.540-522C>A	XP_011516735.1:n.540-522C>A
XM_011518434.1:c.501-522C>A	XP_011516736.1:n.501-522C>A
XM_011518435.1:c.540-522C>A	XP_011516737.1:n.540-522C>A
XM_011518436.1:c.666C>A	XP_011516738.1:p.Phe222Leu
XM_017014561.2:c.627C>A	XP_016870050.1:p.Phe209Leu
XM_017014562.2:c.627C>A	XP_016870051.1:p.Phe209Leu
XM_017014563.2:c.501-522C>A	XP_016870052.1:n.501-522C>A
XM_017014564.2:c.549C>A	XP_016870053.1:p.Phe183Leu
XR_001746263.2:n.868C>A
XR_001746264.2:n.874C>A
XR_001746265.2:n.671C>A
NM_001170639.2:c.549C>A	NP_001164110.1:p.Phe183Leu
NM_001039803.3:c.612C>A MANE Select	NP_001034892.1:p.Phe204Leu
NM_001170640.2:c.501-522C>A	NP_001164111.1:n.501-522C>A
NM_012119.5:c.549C>A	NP_036251.2:p.Phe183Leu
NM_178432.4:c.588C>A	NP_848519.1:p.Phe196Leu