Canonical Allele Identifier: CA2038995103
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750663G= , CM000674.2:g.57750663G= GRCh38
NC_000012.11:g.58144446G= , CM000674.1:g.58144446G= GRCh37
NC_000012.10:g.56430713G= NCBI36
NG_007484.2:g.6719C= , LRG_490:g.6719C=

Transcript Alleles

HGVS Amino-acid change
ENST00000257904.11:c.625C= MANE Select ENSP00000257904.5:p.Arg209=
ENST00000257904.10:c.625C= ENSP00000257904.5:p.Arg209=
ENST00000312990.10:c.273C= ENSP00000316889.6:p.Phe91=
ENST00000546489.5:c.403C= ENSP00000447779.1:p.Arg135=
ENST00000547281.5:c.403C= ENSP00000447274.1:p.Arg135=
ENST00000549606.5:c.-157-1159C= ENSP00000447005.1:n.-157-1159C=
ENST00000550419.5:c.523-100C= ENSP00000448098.1:n.523-100C=
ENST00000551888.5:n.451C=
ENST00000553237.5:c.*264C= ENSP00000448885.1:n.*264C=
NM_000075.3:c.625C= NP_000066.1:p.Arg209=
NM_000075.4:c.625C= MANE Select NP_000066.1:p.Arg209=