Canonical Allele Identifier: CA2038994905
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750615T= , CM000674.2:g.57750615T= GRCh38
NC_000012.11:g.58144398T= , CM000674.1:g.58144398T= GRCh37
NC_000012.10:g.56430665T= NCBI36
NG_007484.2:g.6767A= , LRG_490:g.6767A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.632+41A= MANE Select ENSP00000257904.5:n.632+41A=
ENST00000257904.10:c.632+41A= ENSP00000257904.5:n.632+41A=
ENST00000312990.10:c.280+41A= ENSP00000316889.6:n.280+41A=
ENST00000546489.5:c.410+41A= ENSP00000447779.1:n.410+41A=
ENST00000547281.5:c.410+41A= ENSP00000447274.1:n.410+41A=
ENST00000549606.5:c.-157-1111A= ENSP00000447005.1:n.-157-1111A=
ENST00000550419.5:c.523-52A= ENSP00000448098.1:n.523-52A=
ENST00000551888.5:n.458+41A=
ENST00000553237.5:c.*271+41A= ENSP00000448885.1:n.*271+41A=
NM_000075.3:c.632+41A= NP_000066.1:n.632+41A=
NM_000075.4:c.632+41A= MANE Select NP_000066.1:n.632+41A=