Canonical Allele Identifier: CA2575206200

Gene: CDK4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750834C>T , CM000674.2:g.57750834C>T	GRCh38
NC_000012.11:g.58144617C>T , CM000674.1:g.58144617C>T	GRCh37
NC_000012.10:g.56430884C>T	NCBI36
NG_007484.2:g.6548G>A , LRG_490:g.6548G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.523-69G>A MANE Select	ENSP00000257904.5:n.523-69G>A
ENST00000257904.10:c.523-69G>A	ENSP00000257904.5:n.523-69G>A
ENST00000312990.10:c.265-163G>A	ENSP00000316889.6:n.265-163G>A
ENST00000546489.5:c.301-69G>A	ENSP00000447779.1:n.301-69G>A
ENST00000547281.5:c.301-69G>A	ENSP00000447274.1:n.301-69G>A
ENST00000549606.5:c.-157-1330G>A	ENSP00000447005.1:n.-157-1330G>A
ENST00000550419.5:c.522+89G>A	ENSP00000448098.1:n.522+89G>A
ENST00000551706.1:n.977G>A
ENST00000551800.5:c.301-69G>A	ENSP00000449391.1:n.301-69G>A
ENST00000551888.5:n.443-163G>A
ENST00000552254.5:c.523-69G>A	ENSP00000449179.1:n.523-69G>A
ENST00000553237.5:c.*162-69G>A	ENSP00000448885.1:n.*162-69G>A
NM_000075.3:c.523-69G>A	NP_000066.1:n.523-69G>A
NM_000075.4:c.523-69G>A MANE Select	NP_000066.1:n.523-69G>A