Canonical Allele Identifier: CA6657774
Gene: CDK4 HGNC NCBI

Linked Data

ClinVar Variation Id: 463472
dbSNP Id: rs754423955

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750662C>T , CM000674.2:g.57750662C>T GRCh38
NC_000012.11:g.58144445C>T , CM000674.1:g.58144445C>T GRCh37
NC_000012.10:g.56430712C>T NCBI36
NG_007484.2:g.6720G>A , LRG_490:g.6720G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000257904.11:c.626G>A MANE Select ENSP00000257904.5:p.Arg209His
ENST00000257904.10:c.626G>A ENSP00000257904.5:p.Arg209His
ENST00000312990.10:c.274G>A ENSP00000316889.6:p.Val92Ile
ENST00000546489.5:c.404G>A ENSP00000447779.1:p.Arg135His
ENST00000547281.5:c.404G>A ENSP00000447274.1:p.Arg135His
ENST00000549606.5:c.-157-1158G>A ENSP00000447005.1:n.-157-1158G>A
ENST00000550419.5:c.523-99G>A ENSP00000448098.1:n.523-99G>A
ENST00000551888.5:n.452G>A
ENST00000553237.5:c.*265G>A ENSP00000448885.1:n.*265G>A
NM_000075.3:c.626G>A NP_000066.1:p.Arg209His
NM_000075.4:c.626G>A MANE Select NP_000066.1:p.Arg209His