Canonical Allele Identifier: CA2038995170
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750689A= , CM000674.2:g.57750689A= GRCh38
NC_000012.11:g.58144472A= , CM000674.1:g.58144472A= GRCh37
NC_000012.10:g.56430739A= NCBI36
NG_007484.2:g.6693T= , LRG_490:g.6693T=

Transcript Alleles

HGVS Amino-acid change
ENST00000257904.11:c.599T= MANE Select ENSP00000257904.5:p.Val200=
ENST00000257904.10:c.599T= ENSP00000257904.5:p.Val200=
ENST00000312990.10:c.265-18T= ENSP00000316889.6:n.265-18T=
ENST00000546489.5:c.377T= ENSP00000447779.1:p.Val126=
ENST00000547281.5:c.377T= ENSP00000447274.1:p.Val126=
ENST00000549606.5:c.-157-1185T= ENSP00000447005.1:n.-157-1185T=
ENST00000550419.5:c.523-126T= ENSP00000448098.1:n.523-126T=
ENST00000551800.5:c.377T= ENSP00000449391.1:p.Val126=
ENST00000551888.5:n.443-18T=
ENST00000552254.5:c.599T= ENSP00000449179.1:p.Val200=
ENST00000553237.5:c.*238T= ENSP00000448885.1:n.*238T=
NM_000075.3:c.599T= NP_000066.1:p.Val200=
NM_000075.4:c.599T= MANE Select NP_000066.1:p.Val200=