Canonical Allele Identifier: CA480301063
Gene: CDK4 HGNC NCBI

Linked Data

dbSNP Id: rs2140385667
MyVariant Identifiers: chr12:g.58144468G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750685G>T , CM000674.2:g.57750685G>T GRCh38
NC_000012.11:g.58144468G>T , CM000674.1:g.58144468G>T GRCh37
NC_000012.10:g.56430735G>T NCBI36
NG_007484.2:g.6697C>A , LRG_490:g.6697C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000257904.11:c.603C>A MANE Select ENSP00000257904.5:p.Gly201=
ENST00000257904.10:c.603C>A ENSP00000257904.5:p.Gly201=
ENST00000312990.10:c.265-14C>A ENSP00000316889.6:n.265-14C>A
ENST00000546489.5:c.381C>A ENSP00000447779.1:p.Gly127=
ENST00000547281.5:c.381C>A ENSP00000447274.1:p.Gly127=
ENST00000549606.5:c.-157-1181C>A ENSP00000447005.1:n.-157-1181C>A
ENST00000550419.5:c.523-122C>A ENSP00000448098.1:n.523-122C>A
ENST00000551800.5:c.381C>A ENSP00000449391.1:p.Gly127=
ENST00000551888.5:n.443-14C>A
ENST00000552254.5:c.603C>A ENSP00000449179.1:p.Gly201=
ENST00000553237.5:c.*242C>A ENSP00000448885.1:n.*242C>A
NM_000075.3:c.603C>A NP_000066.1:p.Gly201=
NM_000075.4:c.603C>A MANE Select NP_000066.1:p.Gly201=