Canonical Allele Identifier: CA655040472

Gene: CDK4

Linked Data

• COSMIC: COSN20081684

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750565_57750566insA , CM000674.2:g.57750565_57750566insA	GRCh38
NC_000012.11:g.58144348_58144349insA , CM000674.1:g.58144348_58144349insA	GRCh37
NC_000012.10:g.56430615_56430616insA	NCBI36
NG_007484.2:g.6816_6817insT , LRG_490:g.6816_6817insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.632+90_632+91insT MANE Select	ENSP00000257904.5:n.632+90_632+91insT
ENST00000257904.10:c.632+90_632+91insT	ENSP00000257904.5:n.632+90_632+91insT
ENST00000312990.10:c.280+90_280+91insT	ENSP00000316889.6:n.280+90_280+91insT
ENST00000546489.5:c.410+90_410+91insT	ENSP00000447779.1:n.410+90_410+91insT
ENST00000547281.5:c.410+90_410+91insT	ENSP00000447274.1:n.410+90_410+91insT
ENST00000549606.5:c.-157-1062_-157-1061insT	ENSP00000447005.1:n.-157-1062_-157-1061insT
ENST00000550419.5:c.523-3_523-2insT	ENSP00000448098.1:n.523-3_523-2insT
ENST00000551888.5:n.458+90_458+91insT
ENST00000553237.5:c.*271+90_*271+91insT	ENSP00000448885.1:n.*271+90_*271+91insT
NM_000075.3:c.632+90_632+91insT	NP_000066.1:n.632+90_632+91insT
NM_000075.4:c.632+90_632+91insT MANE Select	NP_000066.1:n.632+90_632+91insT