Canonical Allele Identifier: CA2038995086
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750660G= , CM000674.2:g.57750660G= GRCh38
NC_000012.11:g.58144443G= , CM000674.1:g.58144443G= GRCh37
NC_000012.10:g.56430710G= NCBI36
NG_007484.2:g.6722C= , LRG_490:g.6722C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.628C= MANE Select ENSP00000257904.5:p.Arg210=
ENST00000257904.10:c.628C= ENSP00000257904.5:p.Arg210=
ENST00000312990.10:c.276C= ENSP00000316889.6:p.Val92=
ENST00000546489.5:c.406C= ENSP00000447779.1:p.Arg136=
ENST00000547281.5:c.406C= ENSP00000447274.1:p.Arg136=
ENST00000549606.5:c.-157-1156C= ENSP00000447005.1:n.-157-1156C=
ENST00000550419.5:c.523-97C= ENSP00000448098.1:n.523-97C=
ENST00000551888.5:n.454C=
ENST00000553237.5:c.*267C= ENSP00000448885.1:n.*267C=
NM_000075.3:c.628C= NP_000066.1:p.Arg210=
NM_000075.4:c.628C= MANE Select NP_000066.1:p.Arg210=