Canonical Allele Identifier: CA6657777

Gene: CDK4

Linked Data

• ClinVar Variation Id: 825952
• ClinVar RCV Id: RCV001024505
• dbSNP Id: rs565563672
• ExAC: 12:58144495 T / G
• gnomAD v2: 12-58144495-T-G
• gnomAD v3: 12-57750712-T-G
• gnomAD v4: 12-57750712-T-G
• MyVariant Identifiers: chr12:g.58144495T>G (hg19) ; chr12:g.57750712T>G (hg38)

Genomic Alleles

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

Transcript Alleles

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