Canonical Allele Identifier: CA16606362
Gene: CDK4 HGNC NCBI

Linked Data

ClinVar Variation Id: 389605
ClinVar RCV Id: RCV000428875
dbSNP Id: rs1057523487

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57751640G>A , CM000674.2:g.57751640G>A GRCh38
NC_000012.11:g.58145423G>A , CM000674.1:g.58145423G>A GRCh37
NC_000012.10:g.56431690G>A NCBI36
NG_007484.2:g.5742C>T , LRG_490:g.5742C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000257904.11:c.78C>T MANE Select ENSP00000257904.5:p.Pro26=
ENST00000257904.10:c.78C>T ENSP00000257904.5:p.Pro26=
ENST00000312990.10:c.78C>T ENSP00000316889.6:p.Pro26=
ENST00000546489.5:c.-4-298C>T ENSP00000447779.1:n.-4-298C>T
ENST00000547281.5:c.-145C>T ENSP00000447274.1:n.-145C>T
ENST00000549606.5:c.-158+535C>T ENSP00000447005.1:n.-158+535C>T
ENST00000550419.5:c.78C>T ENSP00000448098.1:p.Pro26=
ENST00000551706.1:n.287C>T
ENST00000551800.5:c.-145C>T ENSP00000449391.1:n.-145C>T
ENST00000551888.5:n.256C>T
ENST00000552254.5:c.78C>T ENSP00000449179.1:p.Pro26=
ENST00000552388.1:c.78C>T ENSP00000448963.1:p.Pro26=
ENST00000552862.1:c.78C>T ENSP00000446763.1:p.Pro26=
ENST00000553237.5:c.78C>T ENSP00000448885.1:p.Pro26=
NM_000075.3:c.78C>T NP_000066.1:p.Pro26=
NM_000075.4:c.78C>T MANE Select NP_000066.1:p.Pro26=