Canonical Allele Identifier: CA2038995718
Gene: CDK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750929T= , CM000674.2:g.57750929T= GRCh38
NC_000012.11:g.58144712T= , CM000674.1:g.58144712T= GRCh37
NC_000012.10:g.56430979T= NCBI36
NG_007484.2:g.6453A= , LRG_490:g.6453A=

Transcript Alleles

HGVS Amino-acid change
ENST00000257904.11:c.516A= MANE Select ENSP00000257904.5:p.Thr172=
ENST00000257904.10:c.516A= ENSP00000257904.5:p.Thr172=
ENST00000312990.10:c.265-258A= ENSP00000316889.6:n.265-258A=
ENST00000546489.5:c.294A= ENSP00000447779.1:p.Thr98=
ENST00000547281.5:c.294A= ENSP00000447274.1:p.Thr98=
ENST00000549606.5:c.-158+1246A= ENSP00000447005.1:n.-158+1246A=
ENST00000550419.5:c.516A= ENSP00000448098.1:p.Thr172=
ENST00000551706.1:n.882A=
ENST00000551800.5:c.294A= ENSP00000449391.1:p.Thr98=
ENST00000551888.5:n.443-258A=
ENST00000552254.5:c.516A= ENSP00000449179.1:p.Thr172=
ENST00000553237.5:c.*155A= ENSP00000448885.1:n.*155A=
NM_000075.3:c.516A= NP_000066.1:p.Thr172=
NM_000075.4:c.516A= MANE Select NP_000066.1:p.Thr172=