Canonical Allele Identifier: CA2038995099
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750662C= , CM000674.2:g.57750662C= GRCh38
NC_000012.11:g.58144445C= , CM000674.1:g.58144445C= GRCh37
NC_000012.10:g.56430712C= NCBI36
NG_007484.2:g.6720G= , LRG_490:g.6720G=

Transcript Alleles

HGVS Amino-acid change
ENST00000257904.11:c.626G= MANE Select ENSP00000257904.5:p.Arg209=
ENST00000257904.10:c.626G= ENSP00000257904.5:p.Arg209=
ENST00000312990.10:c.274G= ENSP00000316889.6:p.Val92=
ENST00000546489.5:c.404G= ENSP00000447779.1:p.Arg135=
ENST00000547281.5:c.404G= ENSP00000447274.1:p.Arg135=
ENST00000549606.5:c.-157-1158G= ENSP00000447005.1:n.-157-1158G=
ENST00000550419.5:c.523-99G= ENSP00000448098.1:n.523-99G=
ENST00000551888.5:n.452G=
ENST00000553237.5:c.*265G= ENSP00000448885.1:n.*265G=
NM_000075.3:c.626G= NP_000066.1:p.Arg209=
NM_000075.4:c.626G= MANE Select NP_000066.1:p.Arg209=