Canonical Allele Identifier: CA385546402
Gene: CDK4 HGNC NCBI

Linked Data

ClinVar Variation Id: 483279
dbSNP Id: rs1443076952

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750987G>A , CM000674.2:g.57750987G>A GRCh38
NC_000012.11:g.58144770G>A , CM000674.1:g.58144770G>A GRCh37
NC_000012.10:g.56431037G>A NCBI36
NG_007484.2:g.6395C>T , LRG_490:g.6395C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000257904.11:c.458C>T MANE Select ENSP00000257904.5:p.Thr153Ile
ENST00000257904.10:c.458C>T ENSP00000257904.5:p.Thr153Ile
ENST00000312990.10:c.264+310C>T ENSP00000316889.6:n.264+310C>T
ENST00000546489.5:c.236C>T ENSP00000447779.1:p.Thr79Ile
ENST00000547281.5:c.236C>T ENSP00000447274.1:p.Thr79Ile
ENST00000549606.5:c.-158+1188C>T ENSP00000447005.1:n.-158+1188C>T
ENST00000550419.5:c.458C>T ENSP00000448098.1:p.Thr153Ile
ENST00000551706.1:n.824C>T
ENST00000551800.5:c.236C>T ENSP00000449391.1:p.Thr79Ile
ENST00000551888.5:n.442+310C>T
ENST00000552254.5:c.458C>T ENSP00000449179.1:p.Thr153Ile
ENST00000552388.1:c.458C>T ENSP00000448963.1:p.Thr153Ile
ENST00000553237.5:c.*97C>T ENSP00000448885.1:n.*97C>T
NM_000075.3:c.458C>T NP_000066.1:p.Thr153Ile
NM_000075.4:c.458C>T MANE Select NP_000066.1:p.Thr153Ile