Canonical Allele Identifier: CA2038994368
Gene: CDK4 HGNC NCBI

Linked Data

dbSNP Id: rs1955220701
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750272A>G , CM000674.2:g.57750272A>G GRCh38
NC_000012.11:g.58144055A>G , CM000674.1:g.58144055A>G GRCh37
NC_000012.10:g.56430322A>G NCBI36
NG_007484.2:g.7110T>C , LRG_490:g.7110T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.632+384T>C MANE Select ENSP00000257904.5:n.632+384T>C
ENST00000257904.10:c.632+384T>C ENSP00000257904.5:n.632+384T>C
ENST00000312990.10:c.280+384T>C ENSP00000316889.6:n.280+384T>C
ENST00000546489.5:c.410+384T>C ENSP00000447779.1:n.410+384T>C
ENST00000547281.5:c.410+384T>C ENSP00000447274.1:n.410+384T>C
ENST00000549606.5:c.-157-768T>C ENSP00000447005.1:n.-157-768T>C
ENST00000550419.5:c.*38+170T>C ENSP00000448098.1:n.*38+170T>C
ENST00000551888.5:n.458+384T>C
ENST00000553237.5:c.*271+384T>C ENSP00000448885.1:n.*271+384T>C
NM_000075.3:c.632+384T>C NP_000066.1:n.632+384T>C
NM_000075.4:c.632+384T>C MANE Select NP_000066.1:n.632+384T>C
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