Canonical Allele Identifier: CA480301185

Gene: CDK4

Linked Data

• dbSNP Id: rs565563672
• MyVariant Identifiers: chr12:g.58144495T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750712T>A , CM000674.2:g.57750712T>A	GRCh38
NC_000012.11:g.58144495T>A , CM000674.1:g.58144495T>A	GRCh37
NC_000012.10:g.56430762T>A	NCBI36
NG_007484.2:g.6670A>T , LRG_490:g.6670A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.576A>T MANE Select	ENSP00000257904.5:p.Ala192=
ENST00000257904.10:c.576A>T	ENSP00000257904.5:p.Ala192=
ENST00000312990.10:c.265-41A>T	ENSP00000316889.6:n.265-41A>T
ENST00000546489.5:c.354A>T	ENSP00000447779.1:p.Ala118=
ENST00000547281.5:c.354A>T	ENSP00000447274.1:p.Ala118=
ENST00000549606.5:c.-157-1208A>T	ENSP00000447005.1:n.-157-1208A>T
ENST00000550419.5:c.523-149A>T	ENSP00000448098.1:n.523-149A>T
ENST00000551800.5:c.354A>T	ENSP00000449391.1:p.Ala118=
ENST00000551888.5:n.443-41A>T
ENST00000552254.5:c.576A>T	ENSP00000449179.1:p.Ala192=
ENST00000553237.5:c.*215A>T	ENSP00000448885.1:n.*215A>T
NM_000075.3:c.576A>T	NP_000066.1:p.Ala192=
NM_000075.4:c.576A>T MANE Select	NP_000066.1:p.Ala192=