Canonical Allele Identifier: CA2726352752
Gene: CDK4 HGNC NCBI

Linked Data

dbSNP Id: rs2140385905

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750764_57750765del , CM000674.2:g.57750764_57750765del GRCh38
NC_000012.11:g.58144547_58144548del , CM000674.1:g.58144547_58144548del GRCh37
NC_000012.10:g.56430814_56430815del NCBI36
NG_007484.2:g.6617_6618del , LRG_490:g.6617_6618del

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.523_524del MANE Select ENSP00000257904.5:p.Val175CysfsTer?
ENST00000257904.10:c.523_524del ENSP00000257904.5:p.Val175CysfsTer?
ENST00000312990.10:c.265-94_265-93del ENSP00000316889.6:n.265-94_265-93del
ENST00000546489.5:c.301_302del ENSP00000447779.1:p.Val101CysfsTer?
ENST00000547281.5:c.301_302del ENSP00000447274.1:p.Val101CysfsTer?
ENST00000549606.5:c.-157-1261_-157-1260del ENSP00000447005.1:n.-157-1261_-157-1260del
ENST00000550419.5:c.522+158_522+159del ENSP00000448098.1:n.522+158_522+159del
ENST00000551800.5:c.301_302del ENSP00000449391.1:p.Val101CysfsTer?
ENST00000551888.5:n.443-94_443-93del
ENST00000552254.5:c.523_524del ENSP00000449179.1:p.Val175CysfsTer?
ENST00000553237.5:c.*162_*163del ENSP00000448885.1:n.*162_*163del
NM_000075.3:c.523_524del NP_000066.1:p.Val175CysfsTer?
NM_000075.4:c.523_524del MANE Select NP_000066.1:p.Val175CysfsTer?