Canonical Allele Identifier: CA385545539

Gene: CDK4

Linked Data

• MyVariant Identifiers: chr12:g.58144446G>T (hg19) ; chr12:g.57750663G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750663G>T , CM000674.2:g.57750663G>T	GRCh38
NC_000012.11:g.58144446G>T , CM000674.1:g.58144446G>T	GRCh37
NC_000012.10:g.56430713G>T	NCBI36
NG_007484.2:g.6719C>A , LRG_490:g.6719C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000257904.11:c.625C>A MANE Select	ENSP00000257904.5:p.Arg209Ser
ENST00000257904.10:c.625C>A	ENSP00000257904.5:p.Arg209Ser
ENST00000312990.10:c.273C>A	ENSP00000316889.6:p.Phe91Leu
ENST00000546489.5:c.403C>A	ENSP00000447779.1:p.Arg135Ser
ENST00000547281.5:c.403C>A	ENSP00000447274.1:p.Arg135Ser
ENST00000549606.5:c.-157-1159C>A	ENSP00000447005.1:n.-157-1159C>A
ENST00000550419.5:c.523-100C>A	ENSP00000448098.1:n.523-100C>A
ENST00000551888.5:n.451C>A
ENST00000553237.5:c.*264C>A	ENSP00000448885.1:n.*264C>A
NM_000075.3:c.625C>A	NP_000066.1:p.Arg209Ser
NM_000075.4:c.625C>A MANE Select	NP_000066.1:p.Arg209Ser