Canonical Allele Identifier: CA653349173

Gene: CDK1

Linked Data

• COSMIC: COSN10070736

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.60788715T>G , CM000672.2:g.60788715T>G	GRCh38
NC_000010.10:g.62548473T>G , CM000672.1:g.62548473T>G	GRCh37
NC_000010.9:g.62218479T>G	NCBI36
NG_029877.1:g.15385T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395284.8:c.489+485T>G MANE Select	ENSP00000378699.3:n.489+485T>G
ENST00000316629.8:c.318+2928T>G	ENSP00000325970.4:n.318+2928T>G
ENST00000373809.2:c.318+2928T>G	ENSP00000362915.2:n.318+2928T>G
ENST00000395284.7:c.489+485T>G	ENSP00000378699.3:n.489+485T>G
ENST00000448257.6:c.493+481T>G	ENSP00000397973.2:n.493+481T>G
ENST00000487784.1:n.564+481T>G
ENST00000519078.6:c.489+485T>G	ENSP00000430665.2:n.489+485T>G
ENST00000614696.4:c.489+485T>G	ENSP00000482996.1:n.489+485T>G
NM_001786.4:c.489+485T>G	NP_001777.1:n.489+485T>G
NM_033379.4:c.318+2928T>G	NP_203698.1:n.318+2928T>G
XM_005270303.2:c.489+485T>G	XP_005270360.1:n.489+485T>G
XM_006718082.1:c.489+485T>G	XP_006718145.1:n.489+485T>G
NM_001320918.1:c.489+485T>G	NP_001307847.1:n.489+485T>G
XM_005270303.3:c.489+485T>G	XP_005270360.1:n.489+485T>G
NM_001786.5:c.489+485T>G MANE Select	NP_001777.1:n.489+485T>G
NM_033379.5:c.318+2928T>G	NP_203698.1:n.318+2928T>G