Canonical Allele Identifier: CA16044227

Gene: CDK20

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.87969919C>T , CM000671.2:g.87969919C>T	GRCh38
NC_000009.11:g.90584834C>T , CM000671.1:g.90584834C>T	GRCh37
NC_000009.10:g.89774654C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325303.9:c.564G>A MANE Select	ENSP00000322343.8:p.Trp188Ter
ENST00000325303.8:c.564G>A	ENSP00000322343.8:p.Trp188Ter
ENST00000336654.9:c.540G>A	ENSP00000338975.5:p.Arg180=
ENST00000375871.8:c.501-570G>A	ENSP00000365031.3:n.501-570G>A
ENST00000375883.7:c.501G>A	ENSP00000365043.3:p.Arg167=
ENST00000459720.5:n.1596G>A
ENST00000486228.7:n.964G>A
ENST00000603475.1:n.2030G>A
ENST00000605159.5:c.501G>A	ENSP00000474485.1:p.Arg167=
NM_001039803.2:c.564G>A	NP_001034892.1:p.Trp188Ter
NM_001170639.1:c.501G>A	NP_001164110.1:p.Arg167=
NM_001170640.1:c.501-570G>A	NP_001164111.1:n.501-570G>A
NM_012119.4:c.501G>A	NP_036251.2:p.Arg167=
NM_178432.3:c.540G>A	NP_848519.1:p.Arg180=
XM_011518425.1:c.618G>A	XP_011516727.1:p.Trp206Ter
XM_011518426.1:c.603G>A	XP_011516728.1:p.Trp201Ter
XM_011518427.1:c.579G>A	XP_011516729.1:p.Trp193Ter
XM_011518428.1:c.564G>A	XP_011516730.1:p.Trp188Ter
XM_011518429.1:c.540G>A	XP_011516731.1:p.Arg180=
XM_011518430.1:c.501G>A	XP_011516732.1:p.Arg167=
XM_011518431.1:c.618G>A	XP_011516733.1:p.Trp206Ter
XM_011518432.1:c.603G>A	XP_011516734.1:p.Trp201Ter
XM_011518433.1:c.540-570G>A	XP_011516735.1:n.540-570G>A
XM_011518434.1:c.501-570G>A	XP_011516736.1:n.501-570G>A
XM_011518435.1:c.540-570G>A	XP_011516737.1:n.540-570G>A
XM_011518436.1:c.618G>A	XP_011516738.1:p.Trp206Ter
XM_017014561.2:c.579G>A	XP_016870050.1:p.Trp193Ter
XM_017014562.2:c.579G>A	XP_016870051.1:p.Trp193Ter
XM_017014563.2:c.501-570G>A	XP_016870052.1:n.501-570G>A
XM_017014564.2:c.501G>A	XP_016870053.1:p.Arg167=
XR_001746263.2:n.820G>A
XR_001746264.2:n.826G>A
XR_001746265.2:n.623G>A
NM_001170639.2:c.501G>A	NP_001164110.1:p.Arg167=
NM_001039803.3:c.564G>A MANE Select	NP_001034892.1:p.Trp188Ter
NM_001170640.2:c.501-570G>A	NP_001164111.1:n.501-570G>A
NM_012119.5:c.501G>A	NP_036251.2:p.Arg167=
NM_178432.4:c.540G>A	NP_848519.1:p.Arg180=