Canonical Allele Identifier: CA2726352711
Gene: CDK4 HGNC NCBI

Linked Data

dbSNP Id: rs2140385539

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750639G>C , CM000674.2:g.57750639G>C GRCh38
NC_000012.11:g.58144422G>C , CM000674.1:g.58144422G>C GRCh37
NC_000012.10:g.56430689G>C NCBI36
NG_007484.2:g.6743C>G , LRG_490:g.6743C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.632+17C>G MANE Select ENSP00000257904.5:n.632+17C>G
ENST00000257904.10:c.632+17C>G ENSP00000257904.5:n.632+17C>G
ENST00000312990.10:c.280+17C>G ENSP00000316889.6:n.280+17C>G
ENST00000546489.5:c.410+17C>G ENSP00000447779.1:n.410+17C>G
ENST00000547281.5:c.410+17C>G ENSP00000447274.1:n.410+17C>G
ENST00000549606.5:c.-157-1135C>G ENSP00000447005.1:n.-157-1135C>G
ENST00000550419.5:c.523-76C>G ENSP00000448098.1:n.523-76C>G
ENST00000551888.5:n.458+17C>G
ENST00000553237.5:c.*271+17C>G ENSP00000448885.1:n.*271+17C>G
NM_000075.3:c.632+17C>G NP_000066.1:n.632+17C>G
NM_000075.4:c.632+17C>G MANE Select NP_000066.1:n.632+17C>G