Canonical Allele Identifier: CA2038994627
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750469_57750470delinsAG , CM000674.2:g.57750469_57750470delinsAG GRCh38
NC_000012.11:g.58144252_58144253delinsAG , CM000674.1:g.58144252_58144253delinsAG GRCh37
NC_000012.10:g.56430519_56430520delinsAG NCBI36
NG_007484.2:g.6912_6913delinsCT , LRG_490:g.6912_6913delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.632+186_632+187delinsCT MANE Select ENSP00000257904.5:n.632+186_632+187delinsCT
ENST00000257904.10:c.632+186_632+187delinsCT ENSP00000257904.5:n.632+186_632+187delinsCT
ENST00000312990.10:c.280+186_280+187delinsCT ENSP00000316889.6:n.280+186_280+187delinsCT
ENST00000546489.5:c.410+186_410+187delinsCT ENSP00000447779.1:n.410+186_410+187delinsCT
ENST00000547281.5:c.410+186_410+187delinsCT ENSP00000447274.1:n.410+186_410+187delinsCT
ENST00000549606.5:c.-157-966_-157-965delinsCT ENSP00000447005.1:n.-157-966_-157-965delinsCT
ENST00000550419.5:c.*10_*11delinsCT ENSP00000448098.1:n.*10_*11delinsCT
ENST00000551888.5:n.458+186_458+187delinsCT
ENST00000553237.5:c.*271+186_*271+187delinsCT ENSP00000448885.1:n.*271+186_*271+187delinsCT
NM_000075.3:c.632+186_632+187delinsCT NP_000066.1:n.632+186_632+187delinsCT
NM_000075.4:c.632+186_632+187delinsCT MANE Select NP_000066.1:n.632+186_632+187delinsCT