Canonical Allele Identifier: CA2038995399
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750750A= , CM000674.2:g.57750750A= GRCh38
NC_000012.11:g.58144533A= , CM000674.1:g.58144533A= GRCh37
NC_000012.10:g.56430800A= NCBI36
NG_007484.2:g.6632T= , LRG_490:g.6632T=

Transcript Alleles

HGVS Amino-acid change
ENST00000257904.11:c.538T= MANE Select ENSP00000257904.5:p.Tyr180=
ENST00000257904.10:c.538T= ENSP00000257904.5:p.Tyr180=
ENST00000312990.10:c.265-79T= ENSP00000316889.6:n.265-79T=
ENST00000546489.5:c.316T= ENSP00000447779.1:p.Tyr106=
ENST00000547281.5:c.316T= ENSP00000447274.1:p.Tyr106=
ENST00000549606.5:c.-157-1246T= ENSP00000447005.1:n.-157-1246T=
ENST00000550419.5:c.522+173T= ENSP00000448098.1:n.522+173T=
ENST00000551800.5:c.316T= ENSP00000449391.1:p.Tyr106=
ENST00000551888.5:n.443-79T=
ENST00000552254.5:c.538T= ENSP00000449179.1:p.Tyr180=
ENST00000553237.5:c.*177T= ENSP00000448885.1:n.*177T=
NM_000075.3:c.538T= NP_000066.1:p.Tyr180=
NM_000075.4:c.538T= MANE Select NP_000066.1:p.Tyr180=