Canonical Allele Identifier: CA2038994468
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750336T= , CM000674.2:g.57750336T= GRCh38
NC_000012.11:g.58144119T= , CM000674.1:g.58144119T= GRCh37
NC_000012.10:g.56430386T= NCBI36
NG_007484.2:g.7046A= , LRG_490:g.7046A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.632+320A= MANE Select ENSP00000257904.5:n.632+320A=
ENST00000257904.10:c.632+320A= ENSP00000257904.5:n.632+320A=
ENST00000312990.10:c.280+320A= ENSP00000316889.6:n.280+320A=
ENST00000546489.5:c.410+320A= ENSP00000447779.1:n.410+320A=
ENST00000547281.5:c.410+320A= ENSP00000447274.1:n.410+320A=
ENST00000549606.5:c.-157-832A= ENSP00000447005.1:n.-157-832A=
ENST00000550419.5:c.*38+106A= ENSP00000448098.1:n.*38+106A=
ENST00000551888.5:n.458+320A=
ENST00000553237.5:c.*271+320A= ENSP00000448885.1:n.*271+320A=
NM_000075.3:c.632+320A= NP_000066.1:n.632+320A=
NM_000075.4:c.632+320A= MANE Select NP_000066.1:n.632+320A=