Canonical Allele Identifier: CA385545675

Gene: CDK4

Linked Data

• COSMIC: COSM1578941
• MyVariant Identifiers: chr12:g.58144470C>G (hg19) ; chr12:g.57750687C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750687C>G , CM000674.2:g.57750687C>G	GRCh38
NC_000012.11:g.58144470C>G , CM000674.1:g.58144470C>G	GRCh37
NC_000012.10:g.56430737C>G	NCBI36
NG_007484.2:g.6695G>C , LRG_490:g.6695G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000257904.11:c.601G>C MANE Select	ENSP00000257904.5:p.Gly201Arg
ENST00000257904.10:c.601G>C	ENSP00000257904.5:p.Gly201Arg
ENST00000312990.10:c.265-16G>C	ENSP00000316889.6:n.265-16G>C
ENST00000546489.5:c.379G>C	ENSP00000447779.1:p.Gly127Arg
ENST00000547281.5:c.379G>C	ENSP00000447274.1:p.Gly127Arg
ENST00000549606.5:c.-157-1183G>C	ENSP00000447005.1:n.-157-1183G>C
ENST00000550419.5:c.523-124G>C	ENSP00000448098.1:n.523-124G>C
ENST00000551800.5:c.379G>C	ENSP00000449391.1:p.Gly127Arg
ENST00000551888.5:n.443-16G>C
ENST00000552254.5:c.601G>C	ENSP00000449179.1:p.Gly201Arg
ENST00000553237.5:c.*240G>C	ENSP00000448885.1:n.*240G>C
NM_000075.3:c.601G>C	NP_000066.1:p.Gly201Arg
NM_000075.4:c.601G>C MANE Select	NP_000066.1:p.Gly201Arg