Canonical Allele Identifier: CA2038995111
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750668A= , CM000674.2:g.57750668A= GRCh38
NC_000012.11:g.58144451A= , CM000674.1:g.58144451A= GRCh37
NC_000012.10:g.56430718A= NCBI36
NG_007484.2:g.6714T= , LRG_490:g.6714T=

Transcript Alleles

HGVS Amino-acid change
ENST00000257904.11:c.620T= MANE Select ENSP00000257904.5:p.Met207=
ENST00000257904.10:c.620T= ENSP00000257904.5:p.Met207=
ENST00000312990.10:c.268T= ENSP00000316889.6:p.Cys90=
ENST00000546489.5:c.398T= ENSP00000447779.1:p.Met133=
ENST00000547281.5:c.398T= ENSP00000447274.1:p.Met133=
ENST00000549606.5:c.-157-1164T= ENSP00000447005.1:n.-157-1164T=
ENST00000550419.5:c.523-105T= ENSP00000448098.1:n.523-105T=
ENST00000551888.5:n.446T=
ENST00000553237.5:c.*259T= ENSP00000448885.1:n.*259T=
NM_000075.3:c.620T= NP_000066.1:p.Met207=
NM_000075.4:c.620T= MANE Select NP_000066.1:p.Met207=