Canonical Allele Identifier: CA480404832
Gene: CDK4 HGNC NCBI

Linked Data

ClinVar Variation Id: 485494
dbSNP Id: rs1555201367

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57751538C>T , CM000674.2:g.57751538C>T GRCh38
NC_000012.11:g.58145321C>T , CM000674.1:g.58145321C>T GRCh37
NC_000012.10:g.56431588C>T NCBI36
NG_007484.2:g.5844G>A , LRG_490:g.5844G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000257904.11:c.180G>A MANE Select ENSP00000257904.5:p.Leu60=
ENST00000257904.10:c.180G>A ENSP00000257904.5:p.Leu60=
ENST00000312990.10:c.180G>A ENSP00000316889.6:p.Leu60=
ENST00000546489.5:c.-4-196G>A ENSP00000447779.1:n.-4-196G>A
ENST00000547281.5:c.-43G>A ENSP00000447274.1:n.-43G>A
ENST00000549606.5:c.-158+637G>A ENSP00000447005.1:n.-158+637G>A
ENST00000550419.5:c.180G>A ENSP00000448098.1:p.Leu60=
ENST00000551706.1:n.389G>A
ENST00000551800.5:c.-43G>A ENSP00000449391.1:n.-43G>A
ENST00000551888.5:n.358G>A
ENST00000552254.5:c.180G>A ENSP00000449179.1:p.Leu60=
ENST00000552388.1:c.180G>A ENSP00000448963.1:p.Leu60=
ENST00000552862.1:c.180G>A ENSP00000446763.1:p.Leu60=
ENST00000553237.5:c.180G>A ENSP00000448885.1:p.Leu60=
NM_000075.3:c.180G>A NP_000066.1:p.Leu60=
NM_000075.4:c.180G>A MANE Select NP_000066.1:p.Leu60=