Canonical Allele Identifier: CA915948426
Gene: CDK4 HGNC NCBI

Linked Data

ClinVar Variation Id: 825564
ClinVar RCV Id: RCV001023757
dbSNP Id: rs1595110395

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750919T>C , CM000674.2:g.57750919T>C GRCh38
NC_000012.11:g.58144702T>C , CM000674.1:g.58144702T>C GRCh37
NC_000012.10:g.56430969T>C NCBI36
NG_007484.2:g.6463A>G , LRG_490:g.6463A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.522+4A>G MANE Select ENSP00000257904.5:n.522+4A>G
ENST00000257904.10:c.522+4A>G ENSP00000257904.5:n.522+4A>G
ENST00000312990.10:c.265-248A>G ENSP00000316889.6:n.265-248A>G
ENST00000546489.5:c.300+4A>G ENSP00000447779.1:n.300+4A>G
ENST00000547281.5:c.300+4A>G ENSP00000447274.1:n.300+4A>G
ENST00000549606.5:c.-158+1256A>G ENSP00000447005.1:n.-158+1256A>G
ENST00000550419.5:c.522+4A>G ENSP00000448098.1:n.522+4A>G
ENST00000551706.1:n.892A>G
ENST00000551800.5:c.300+4A>G ENSP00000449391.1:n.300+4A>G
ENST00000551888.5:n.443-248A>G
ENST00000552254.5:c.522+4A>G ENSP00000449179.1:n.522+4A>G
ENST00000553237.5:c.*161+4A>G ENSP00000448885.1:n.*161+4A>G
NM_000075.3:c.522+4A>G NP_000066.1:n.522+4A>G
NM_000075.4:c.522+4A>G MANE Select NP_000066.1:n.522+4A>G