Canonical Allele Identifier: CA6657780
Gene: CDK4 HGNC NCBI

Linked Data

ClinVar Variation Id: 414919
dbSNP Id: rs745772539

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750745T>G , CM000674.2:g.57750745T>G GRCh38
NC_000012.11:g.58144528T>G , CM000674.1:g.58144528T>G GRCh37
NC_000012.10:g.56430795T>G NCBI36
NG_007484.2:g.6637A>C , LRG_490:g.6637A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000257904.11:c.543A>C MANE Select ENSP00000257904.5:p.Arg181=
ENST00000257904.10:c.543A>C ENSP00000257904.5:p.Arg181=
ENST00000312990.10:c.265-74A>C ENSP00000316889.6:n.265-74A>C
ENST00000546489.5:c.321A>C ENSP00000447779.1:p.Arg107=
ENST00000547281.5:c.321A>C ENSP00000447274.1:p.Arg107=
ENST00000549606.5:c.-157-1241A>C ENSP00000447005.1:n.-157-1241A>C
ENST00000550419.5:c.522+178A>C ENSP00000448098.1:n.522+178A>C
ENST00000551800.5:c.321A>C ENSP00000449391.1:p.Arg107=
ENST00000551888.5:n.443-74A>C
ENST00000552254.5:c.543A>C ENSP00000449179.1:p.Arg181=
ENST00000553237.5:c.*182A>C ENSP00000448885.1:n.*182A>C
NM_000075.3:c.543A>C NP_000066.1:p.Arg181=
NM_000075.4:c.543A>C MANE Select NP_000066.1:p.Arg181=