Canonical Allele Identifier: CA2038995439
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750765C= , CM000674.2:g.57750765C= GRCh38
NC_000012.11:g.58144548C= , CM000674.1:g.58144548C= GRCh37
NC_000012.10:g.56430815C= NCBI36
NG_007484.2:g.6617G= , LRG_490:g.6617G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.523G= MANE Select ENSP00000257904.5:p.Val175=
ENST00000257904.10:c.523G= ENSP00000257904.5:p.Val175=
ENST00000312990.10:c.265-94G= ENSP00000316889.6:n.265-94G=
ENST00000546489.5:c.301G= ENSP00000447779.1:p.Val101=
ENST00000547281.5:c.301G= ENSP00000447274.1:p.Val101=
ENST00000549606.5:c.-157-1261G= ENSP00000447005.1:n.-157-1261G=
ENST00000550419.5:c.522+158G= ENSP00000448098.1:n.522+158G=
ENST00000551800.5:c.301G= ENSP00000449391.1:p.Val101=
ENST00000551888.5:n.443-94G=
ENST00000552254.5:c.523G= ENSP00000449179.1:p.Val175=
ENST00000553237.5:c.*162G= ENSP00000448885.1:n.*162G=
NM_000075.3:c.523G= NP_000066.1:p.Val175=
NM_000075.4:c.523G= MANE Select NP_000066.1:p.Val175=