Canonical Allele Identifier: CA385545939

Gene: CDK4

Linked Data

• ClinVar Variation Id: 1424624
• ClinVar RCV Id: RCV001957220
• dbSNP Id: rs772079285
• MyVariant Identifiers: chr12:g.58144529C>G (hg19) ; chr12:g.57750746C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750746C>G , CM000674.2:g.57750746C>G	GRCh38
NC_000012.11:g.58144529C>G , CM000674.1:g.58144529C>G	GRCh37
NC_000012.10:g.56430796C>G	NCBI36
NG_007484.2:g.6636G>C , LRG_490:g.6636G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.542G>C MANE Select	ENSP00000257904.5:p.Arg181Pro
ENST00000257904.10:c.542G>C	ENSP00000257904.5:p.Arg181Pro
ENST00000312990.10:c.265-75G>C	ENSP00000316889.6:n.265-75G>C
ENST00000546489.5:c.320G>C	ENSP00000447779.1:p.Arg107Pro
ENST00000547281.5:c.320G>C	ENSP00000447274.1:p.Arg107Pro
ENST00000549606.5:c.-157-1242G>C	ENSP00000447005.1:n.-157-1242G>C
ENST00000550419.5:c.522+177G>C	ENSP00000448098.1:n.522+177G>C
ENST00000551800.5:c.320G>C	ENSP00000449391.1:p.Arg107Pro
ENST00000551888.5:n.443-75G>C
ENST00000552254.5:c.542G>C	ENSP00000449179.1:p.Arg181Pro
ENST00000553237.5:c.*181G>C	ENSP00000448885.1:n.*181G>C
NM_000075.3:c.542G>C	NP_000066.1:p.Arg181Pro
NM_000075.4:c.542G>C MANE Select	NP_000066.1:p.Arg181Pro