Canonical Allele Identifier: CA2038997862
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57752195T= , CM000674.2:g.57752195T= GRCh38
NC_000012.11:g.58145978T= , CM000674.1:g.58145978T= GRCh37
NC_000012.10:g.56432245T= NCBI36
NG_007484.2:g.5187A= , LRG_490:g.5187A=

Transcript Alleles

HGVS Amino-acid change
ENST00000257904.11:c.-40A= MANE Select ENSP00000257904.5:n.-40A=
ENST00000257904.10:c.-40A= ENSP00000257904.5:n.-40A=
ENST00000312990.10:c.-40A= ENSP00000316889.6:n.-40A=
ENST00000546489.5:c.-25A= ENSP00000447779.1:n.-25A=
ENST00000547281.5:c.-185A= ENSP00000447274.1:n.-185A=
ENST00000549606.5:c.-178A= ENSP00000447005.1:n.-178A=
ENST00000550419.5:c.-40A= ENSP00000448098.1:n.-40A=
ENST00000551706.1:n.170A=
ENST00000551800.5:c.-222A= ENSP00000449391.1:n.-222A=
ENST00000551888.5:n.139A=
ENST00000552388.1:c.-56A= ENSP00000448963.1:n.-56A=
ENST00000552862.1:c.-19-459A= ENSP00000446763.1:n.-19-459A=
ENST00000553237.5:c.-40A= ENSP00000448885.1:n.-40A=
NM_000075.3:c.-40A= NP_000066.1:n.-40A=
NM_000075.4:c.-40A= MANE Select NP_000066.1:n.-40A=