Canonical Allele Identifier: CA2619494809
Gene: CDK4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750827G>T , CM000674.2:g.57750827G>T GRCh38
NC_000012.11:g.58144610G>T , CM000674.1:g.58144610G>T GRCh37
NC_000012.10:g.56430877G>T NCBI36
NG_007484.2:g.6555C>A , LRG_490:g.6555C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000257904.11:c.523-62C>A MANE Select ENSP00000257904.5:n.523-62C>A
ENST00000257904.10:c.523-62C>A ENSP00000257904.5:n.523-62C>A
ENST00000312990.10:c.265-156C>A ENSP00000316889.6:n.265-156C>A
ENST00000546489.5:c.301-62C>A ENSP00000447779.1:n.301-62C>A
ENST00000547281.5:c.301-62C>A ENSP00000447274.1:n.301-62C>A
ENST00000549606.5:c.-157-1323C>A ENSP00000447005.1:n.-157-1323C>A
ENST00000550419.5:c.522+96C>A ENSP00000448098.1:n.522+96C>A
ENST00000551706.1:n.984C>A
ENST00000551800.5:c.301-62C>A ENSP00000449391.1:n.301-62C>A
ENST00000551888.5:n.443-156C>A
ENST00000552254.5:c.523-62C>A ENSP00000449179.1:n.523-62C>A
ENST00000553237.5:c.*162-62C>A ENSP00000448885.1:n.*162-62C>A
NM_000075.3:c.523-62C>A NP_000066.1:n.523-62C>A
NM_000075.4:c.523-62C>A MANE Select NP_000066.1:n.523-62C>A