Canonical Allele Identifier: CA2038994466
Gene: CDK4 HGNC NCBI

Linked Data

dbSNP Id: rs541263133

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750336T>C , CM000674.2:g.57750336T>C GRCh38
NC_000012.11:g.58144119T>C , CM000674.1:g.58144119T>C GRCh37
NC_000012.10:g.56430386T>C NCBI36
NG_007484.2:g.7046A>G , LRG_490:g.7046A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.632+320A>G MANE Select ENSP00000257904.5:n.632+320A>G
ENST00000257904.10:c.632+320A>G ENSP00000257904.5:n.632+320A>G
ENST00000312990.10:c.280+320A>G ENSP00000316889.6:n.280+320A>G
ENST00000546489.5:c.410+320A>G ENSP00000447779.1:n.410+320A>G
ENST00000547281.5:c.410+320A>G ENSP00000447274.1:n.410+320A>G
ENST00000549606.5:c.-157-832A>G ENSP00000447005.1:n.-157-832A>G
ENST00000550419.5:c.*38+106A>G ENSP00000448098.1:n.*38+106A>G
ENST00000551888.5:n.458+320A>G
ENST00000553237.5:c.*271+320A>G ENSP00000448885.1:n.*271+320A>G
NM_000075.3:c.632+320A>G NP_000066.1:n.632+320A>G
NM_000075.4:c.632+320A>G MANE Select NP_000066.1:n.632+320A>G