Canonical Allele Identifier: CA2038995534
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750838T= , CM000674.2:g.57750838T= GRCh38
NC_000012.11:g.58144621T= , CM000674.1:g.58144621T= GRCh37
NC_000012.10:g.56430888T= NCBI36
NG_007484.2:g.6544A= , LRG_490:g.6544A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.523-73A= MANE Select ENSP00000257904.5:n.523-73A=
ENST00000257904.10:c.523-73A= ENSP00000257904.5:n.523-73A=
ENST00000312990.10:c.265-167A= ENSP00000316889.6:n.265-167A=
ENST00000546489.5:c.301-73A= ENSP00000447779.1:n.301-73A=
ENST00000547281.5:c.301-73A= ENSP00000447274.1:n.301-73A=
ENST00000549606.5:c.-157-1334A= ENSP00000447005.1:n.-157-1334A=
ENST00000550419.5:c.522+85A= ENSP00000448098.1:n.522+85A=
ENST00000551706.1:n.973A=
ENST00000551800.5:c.301-73A= ENSP00000449391.1:n.301-73A=
ENST00000551888.5:n.443-167A=
ENST00000552254.5:c.523-73A= ENSP00000449179.1:n.523-73A=
ENST00000553237.5:c.*162-73A= ENSP00000448885.1:n.*162-73A=
NM_000075.3:c.523-73A= NP_000066.1:n.523-73A=
NM_000075.4:c.523-73A= MANE Select NP_000066.1:n.523-73A=