Canonical Allele Identifier: CA2038994419
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750307G= , CM000674.2:g.57750307G= GRCh38
NC_000012.11:g.58144090G= , CM000674.1:g.58144090G= GRCh37
NC_000012.10:g.56430357G= NCBI36
NG_007484.2:g.7075C= , LRG_490:g.7075C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.632+349C= MANE Select ENSP00000257904.5:n.632+349C=
ENST00000257904.10:c.632+349C= ENSP00000257904.5:n.632+349C=
ENST00000312990.10:c.280+349C= ENSP00000316889.6:n.280+349C=
ENST00000546489.5:c.410+349C= ENSP00000447779.1:n.410+349C=
ENST00000547281.5:c.410+349C= ENSP00000447274.1:n.410+349C=
ENST00000549606.5:c.-157-803C= ENSP00000447005.1:n.-157-803C=
ENST00000550419.5:c.*38+135C= ENSP00000448098.1:n.*38+135C=
ENST00000551888.5:n.458+349C=
ENST00000553237.5:c.*271+349C= ENSP00000448885.1:n.*271+349C=
NM_000075.3:c.632+349C= NP_000066.1:n.632+349C=
NM_000075.4:c.632+349C= MANE Select NP_000066.1:n.632+349C=