Canonical Allele Identifier: CA2038994919
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750624T= , CM000674.2:g.57750624T= GRCh38
NC_000012.11:g.58144407T= , CM000674.1:g.58144407T= GRCh37
NC_000012.10:g.56430674T= NCBI36
NG_007484.2:g.6758A= , LRG_490:g.6758A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.632+32A= MANE Select ENSP00000257904.5:n.632+32A=
ENST00000257904.10:c.632+32A= ENSP00000257904.5:n.632+32A=
ENST00000312990.10:c.280+32A= ENSP00000316889.6:n.280+32A=
ENST00000546489.5:c.410+32A= ENSP00000447779.1:n.410+32A=
ENST00000547281.5:c.410+32A= ENSP00000447274.1:n.410+32A=
ENST00000549606.5:c.-157-1120A= ENSP00000447005.1:n.-157-1120A=
ENST00000550419.5:c.523-61A= ENSP00000448098.1:n.523-61A=
ENST00000551888.5:n.458+32A=
ENST00000553237.5:c.*271+32A= ENSP00000448885.1:n.*271+32A=
NM_000075.3:c.632+32A= NP_000066.1:n.632+32A=
NM_000075.4:c.632+32A= MANE Select NP_000066.1:n.632+32A=