Canonical Allele Identifier: CA2038994757
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750536C= , CM000674.2:g.57750536C= GRCh38
NC_000012.11:g.58144319C= , CM000674.1:g.58144319C= GRCh37
NC_000012.10:g.56430586C= NCBI36
NG_007484.2:g.6846G= , LRG_490:g.6846G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.632+120G= MANE Select ENSP00000257904.5:n.632+120G=
ENST00000257904.10:c.632+120G= ENSP00000257904.5:n.632+120G=
ENST00000312990.10:c.280+120G= ENSP00000316889.6:n.280+120G=
ENST00000546489.5:c.410+120G= ENSP00000447779.1:n.410+120G=
ENST00000547281.5:c.410+120G= ENSP00000447274.1:n.410+120G=
ENST00000549606.5:c.-157-1032G= ENSP00000447005.1:n.-157-1032G=
ENST00000550419.5:c.550G= ENSP00000448098.1:p.Gly184=
ENST00000551888.5:n.458+120G=
ENST00000553237.5:c.*271+120G= ENSP00000448885.1:n.*271+120G=
NM_000075.3:c.632+120G= NP_000066.1:n.632+120G=
NM_000075.4:c.632+120G= MANE Select NP_000066.1:n.632+120G=