Canonical Allele Identifier: CA948106016
Gene: CDK4 HGNC NCBI

Linked Data

dbSNP Id: rs1955220905

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750283A>G , CM000674.2:g.57750283A>G GRCh38
NC_000012.11:g.58144066A>G , CM000674.1:g.58144066A>G GRCh37
NC_000012.10:g.56430333A>G NCBI36
NG_007484.2:g.7099T>C , LRG_490:g.7099T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.632+373T>C MANE Select ENSP00000257904.5:n.632+373T>C
ENST00000257904.10:c.632+373T>C ENSP00000257904.5:n.632+373T>C
ENST00000312990.10:c.280+373T>C ENSP00000316889.6:n.280+373T>C
ENST00000546489.5:c.410+373T>C ENSP00000447779.1:n.410+373T>C
ENST00000547281.5:c.410+373T>C ENSP00000447274.1:n.410+373T>C
ENST00000549606.5:c.-157-779T>C ENSP00000447005.1:n.-157-779T>C
ENST00000550419.5:c.*38+159T>C ENSP00000448098.1:n.*38+159T>C
ENST00000551888.5:n.458+373T>C
ENST00000553237.5:c.*271+373T>C ENSP00000448885.1:n.*271+373T>C
NM_000075.3:c.632+373T>C NP_000066.1:n.632+373T>C
NM_000075.4:c.632+373T>C MANE Select NP_000066.1:n.632+373T>C