Canonical Allele Identifier: CA2038995844
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750962C= , CM000674.2:g.57750962C= GRCh38
NC_000012.11:g.58144745C= , CM000674.1:g.58144745C= GRCh37
NC_000012.10:g.56431012C= NCBI36
NG_007484.2:g.6420G= , LRG_490:g.6420G=

Transcript Alleles

HGVS Amino-acid change
ENST00000257904.11:c.483G= MANE Select ENSP00000257904.5:p.Leu161=
ENST00000257904.10:c.483G= ENSP00000257904.5:p.Leu161=
ENST00000312990.10:c.265-291G= ENSP00000316889.6:n.265-291G=
ENST00000546489.5:c.261G= ENSP00000447779.1:p.Leu87=
ENST00000547281.5:c.261G= ENSP00000447274.1:p.Leu87=
ENST00000549606.5:c.-158+1213G= ENSP00000447005.1:n.-158+1213G=
ENST00000550419.5:c.483G= ENSP00000448098.1:p.Leu161=
ENST00000551706.1:n.849G=
ENST00000551800.5:c.261G= ENSP00000449391.1:p.Leu87=
ENST00000551888.5:n.443-291G=
ENST00000552254.5:c.483G= ENSP00000449179.1:p.Leu161=
ENST00000552388.1:c.483G= ENSP00000448963.1:p.Leu161=
ENST00000553237.5:c.*122G= ENSP00000448885.1:n.*122G=
NM_000075.3:c.483G= NP_000066.1:p.Leu161=
NM_000075.4:c.483G= MANE Select NP_000066.1:p.Leu161=