Canonical Allele Identifier: CA385545803
Gene: CDK4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1436239
dbSNP Id: rs543769986

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750711T>A , CM000674.2:g.57750711T>A GRCh38
NC_000012.11:g.58144494T>A , CM000674.1:g.58144494T>A GRCh37
NC_000012.10:g.56430761T>A NCBI36
NG_007484.2:g.6671A>T , LRG_490:g.6671A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.577A>T MANE Select ENSP00000257904.5:p.Thr193Ser
ENST00000257904.10:c.577A>T ENSP00000257904.5:p.Thr193Ser
ENST00000312990.10:c.265-40A>T ENSP00000316889.6:n.265-40A>T
ENST00000546489.5:c.355A>T ENSP00000447779.1:p.Thr119Ser
ENST00000547281.5:c.355A>T ENSP00000447274.1:p.Thr119Ser
ENST00000549606.5:c.-157-1207A>T ENSP00000447005.1:n.-157-1207A>T
ENST00000550419.5:c.523-148A>T ENSP00000448098.1:n.523-148A>T
ENST00000551800.5:c.355A>T ENSP00000449391.1:p.Thr119Ser
ENST00000551888.5:n.443-40A>T
ENST00000552254.5:c.577A>T ENSP00000449179.1:p.Thr193Ser
ENST00000553237.5:c.*216A>T ENSP00000448885.1:n.*216A>T
NM_000075.3:c.577A>T NP_000066.1:p.Thr193Ser
NM_000075.4:c.577A>T MANE Select NP_000066.1:p.Thr193Ser