Canonical Allele Identifier: CA919097386
Gene: CDK4 HGNC NCBI

Linked Data

dbSNP Id: rs1565806314

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750576del , CM000674.2:g.57750576del GRCh38
NC_000012.11:g.58144359del , CM000674.1:g.58144359del GRCh37
NC_000012.10:g.56430626del NCBI36
NG_007484.2:g.6806del , LRG_490:g.6806del

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.632+80del MANE Select ENSP00000257904.5:n.632+80del
ENST00000257904.10:c.632+80del ENSP00000257904.5:n.632+80del
ENST00000312990.10:c.280+80del ENSP00000316889.6:n.280+80del
ENST00000546489.5:c.410+80del ENSP00000447779.1:n.410+80del
ENST00000547281.5:c.410+80del ENSP00000447274.1:n.410+80del
ENST00000549606.5:c.-157-1072del ENSP00000447005.1:n.-157-1072del
ENST00000550419.5:c.523-13del ENSP00000448098.1:n.523-13del
ENST00000551888.5:n.458+80del
ENST00000553237.5:c.*271+80del ENSP00000448885.1:n.*271+80del
NM_000075.3:c.632+80del NP_000066.1:n.632+80del
NM_000075.4:c.632+80del MANE Select NP_000066.1:n.632+80del