Canonical Allele Identifier: CA385545543
Gene: CDK4 HGNC NCBI

Linked Data

dbSNP Id: rs2140385613

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750664A>T , CM000674.2:g.57750664A>T GRCh38
NC_000012.11:g.58144447A>T , CM000674.1:g.58144447A>T GRCh37
NC_000012.10:g.56430714A>T NCBI36
NG_007484.2:g.6718T>A , LRG_490:g.6718T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000257904.11:c.624T>A MANE Select ENSP00000257904.5:p.Phe208Leu
ENST00000257904.10:c.624T>A ENSP00000257904.5:p.Phe208Leu
ENST00000312990.10:c.272T>A ENSP00000316889.6:p.Phe91Tyr
ENST00000546489.5:c.402T>A ENSP00000447779.1:p.Phe134Leu
ENST00000547281.5:c.402T>A ENSP00000447274.1:p.Phe134Leu
ENST00000549606.5:c.-157-1160T>A ENSP00000447005.1:n.-157-1160T>A
ENST00000550419.5:c.523-101T>A ENSP00000448098.1:n.523-101T>A
ENST00000551888.5:n.450T>A
ENST00000553237.5:c.*263T>A ENSP00000448885.1:n.*263T>A
NM_000075.3:c.624T>A NP_000066.1:p.Phe208Leu
NM_000075.4:c.624T>A MANE Select NP_000066.1:p.Phe208Leu