Canonical Allele Identifier: CA667132296

Gene: CDK1

Linked Data

• dbSNP Id: rs1429650610
• gnomAD v3: 10-60788660-GTTTT-G
• gnomAD v4: 10-60788660-GTTTT-G
• MyVariant Identifiers: chr10:g.62548419_62548422del (hg19) ; chr10:g.60788661_60788664del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.60788661_60788664del , CM000672.2:g.60788661_60788664del	GRCh38
NC_000010.10:g.62548419_62548422del , CM000672.1:g.62548419_62548422del	GRCh37
NC_000010.9:g.62218425_62218428del	NCBI36
NG_029877.1:g.15331_15334del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395284.8:c.489+431_489+434del MANE Select	ENSP00000378699.3:n.489+431_489+434del
ENST00000316629.8:c.318+2874_318+2877del	ENSP00000325970.4:n.318+2874_318+2877del
ENST00000373809.2:c.318+2874_318+2877del	ENSP00000362915.2:n.318+2874_318+2877del
ENST00000395284.7:c.489+431_489+434del	ENSP00000378699.3:n.489+431_489+434del
ENST00000448257.6:c.493+427_493+430del	ENSP00000397973.2:n.493+427_493+430del
ENST00000487784.1:n.564+427_564+430del
ENST00000519078.6:c.489+431_489+434del	ENSP00000430665.2:n.489+431_489+434del
ENST00000614696.4:c.489+431_489+434del	ENSP00000482996.1:n.489+431_489+434del
NM_001786.4:c.489+431_489+434del	NP_001777.1:n.489+431_489+434del
NM_033379.4:c.318+2874_318+2877del	NP_203698.1:n.318+2874_318+2877del
XM_005270303.2:c.489+431_489+434del	XP_005270360.1:n.489+431_489+434del
XM_006718082.1:c.489+431_489+434del	XP_006718145.1:n.489+431_489+434del
NM_001320918.1:c.489+431_489+434del	NP_001307847.1:n.489+431_489+434del
XM_005270303.3:c.489+431_489+434del	XP_005270360.1:n.489+431_489+434del
NM_001786.5:c.489+431_489+434del MANE Select	NP_001777.1:n.489+431_489+434del
NM_033379.5:c.318+2874_318+2877del	NP_203698.1:n.318+2874_318+2877del