Canonical Allele Identifier: CA10642117
Gene: CDK4 HGNC NCBI

Linked Data

ClinVar Variation Id: 309982
ClinVar RCV Id: RCV000375683
dbSNP Id: rs886049717

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57752210T>A , CM000674.2:g.57752210T>A GRCh38
NC_000012.11:g.58145993T>A , CM000674.1:g.58145993T>A GRCh37
NC_000012.10:g.56432260T>A NCBI36
NG_007484.2:g.5172A>T , LRG_490:g.5172A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000257904.11:c.-55A>T MANE Select ENSP00000257904.5:n.-55A>T
ENST00000257904.10:c.-55A>T ENSP00000257904.5:n.-55A>T
ENST00000312990.10:c.-55A>T ENSP00000316889.6:n.-55A>T
ENST00000546489.5:c.-40A>T ENSP00000447779.1:n.-40A>T
ENST00000547281.5:c.-200A>T ENSP00000447274.1:n.-200A>T
ENST00000549606.5:c.-193A>T ENSP00000447005.1:n.-193A>T
ENST00000550419.5:c.-55A>T ENSP00000448098.1:n.-55A>T
ENST00000551706.1:n.155A>T
ENST00000551800.5:c.-237A>T ENSP00000449391.1:n.-237A>T
ENST00000551888.5:n.124A>T
ENST00000552388.1:c.-71A>T ENSP00000448963.1:n.-71A>T
ENST00000552862.1:c.-19-474A>T ENSP00000446763.1:n.-19-474A>T
ENST00000553237.5:c.-55A>T ENSP00000448885.1:n.-55A>T
NM_000075.3:c.-55A>T NP_000066.1:n.-55A>T
NM_000075.4:c.-55A>T MANE Select NP_000066.1:n.-55A>T