Canonical Allele Identifier: CA2038994833

Gene: CDK4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750575_57750576delinsAG , CM000674.2:g.57750575_57750576delinsAG	GRCh38
NC_000012.11:g.58144358_58144359delinsAG , CM000674.1:g.58144358_58144359delinsAG	GRCh37
NC_000012.10:g.56430625_56430626delinsAG	NCBI36
NG_007484.2:g.6806_6807delinsCT , LRG_490:g.6806_6807delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.632+80_632+81delinsCT MANE Select	ENSP00000257904.5:n.632+80_632+81delinsCT
ENST00000257904.10:c.632+80_632+81delinsCT	ENSP00000257904.5:n.632+80_632+81delinsCT
ENST00000312990.10:c.280+80_280+81delinsCT	ENSP00000316889.6:n.280+80_280+81delinsCT
ENST00000546489.5:c.410+80_410+81delinsCT	ENSP00000447779.1:n.410+80_410+81delinsCT
ENST00000547281.5:c.410+80_410+81delinsCT	ENSP00000447274.1:n.410+80_410+81delinsCT
ENST00000549606.5:c.-157-1072_-157-1071delinsCT	ENSP00000447005.1:n.-157-1072_-157-1071delinsCT
ENST00000550419.5:c.523-13_523-12delinsCT	ENSP00000448098.1:n.523-13_523-12delinsCT
ENST00000551888.5:n.458+80_458+81delinsCT
ENST00000553237.5:c.*271+80_*271+81delinsCT	ENSP00000448885.1:n.*271+80_*271+81delinsCT
NM_000075.3:c.632+80_632+81delinsCT	NP_000066.1:n.632+80_632+81delinsCT
NM_000075.4:c.632+80_632+81delinsCT MANE Select	NP_000066.1:n.632+80_632+81delinsCT