Canonical Allele Identifier: CA2038995866
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750969A= , CM000674.2:g.57750969A= GRCh38
NC_000012.11:g.58144752A= , CM000674.1:g.58144752A= GRCh37
NC_000012.10:g.56431019A= NCBI36
NG_007484.2:g.6413T= , LRG_490:g.6413T=

Transcript Alleles

HGVS Amino-acid change
ENST00000257904.11:c.476T= MANE Select ENSP00000257904.5:p.Phe159=
ENST00000257904.10:c.476T= ENSP00000257904.5:p.Phe159=
ENST00000312990.10:c.265-298T= ENSP00000316889.6:n.265-298T=
ENST00000546489.5:c.254T= ENSP00000447779.1:p.Phe85=
ENST00000547281.5:c.254T= ENSP00000447274.1:p.Phe85=
ENST00000549606.5:c.-158+1206T= ENSP00000447005.1:n.-158+1206T=
ENST00000550419.5:c.476T= ENSP00000448098.1:p.Phe159=
ENST00000551706.1:n.842T=
ENST00000551800.5:c.254T= ENSP00000449391.1:p.Phe85=
ENST00000551888.5:n.443-298T=
ENST00000552254.5:c.476T= ENSP00000449179.1:p.Phe159=
ENST00000552388.1:c.476T= ENSP00000448963.1:p.Phe159=
ENST00000553237.5:c.*115T= ENSP00000448885.1:n.*115T=
NM_000075.3:c.476T= NP_000066.1:p.Phe159=
NM_000075.4:c.476T= MANE Select NP_000066.1:p.Phe159=