Canonical Allele Identifier: CA2038994296
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750221A= , CM000674.2:g.57750221A= GRCh38
NC_000012.11:g.58144004A= , CM000674.1:g.58144004A= GRCh37
NC_000012.10:g.56430271A= NCBI36
NG_007484.2:g.7161T= , LRG_490:g.7161T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.632+435T= MANE Select ENSP00000257904.5:n.632+435T=
ENST00000257904.10:c.632+435T= ENSP00000257904.5:n.632+435T=
ENST00000312990.10:c.280+435T= ENSP00000316889.6:n.280+435T=
ENST00000546489.5:c.410+435T= ENSP00000447779.1:n.410+435T=
ENST00000547281.5:c.410+435T= ENSP00000447274.1:n.410+435T=
ENST00000549606.5:c.-157-717T= ENSP00000447005.1:n.-157-717T=
ENST00000550419.5:c.*38+221T= ENSP00000448098.1:n.*38+221T=
ENST00000551888.5:n.458+435T=
ENST00000553237.5:c.*271+435T= ENSP00000448885.1:n.*271+435T=
NM_000075.3:c.632+435T= NP_000066.1:n.632+435T=
NM_000075.4:c.632+435T= MANE Select NP_000066.1:n.632+435T=