Canonical Allele Identifier: CA385546293

Gene: CDK4

Linked Data

• dbSNP Id: rs2140386406
• MyVariant Identifiers: chr12:g.58144751A>T (hg19) ; chr12:g.57750968A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750968A>T , CM000674.2:g.57750968A>T	GRCh38
NC_000012.11:g.58144751A>T , CM000674.1:g.58144751A>T	GRCh37
NC_000012.10:g.56431018A>T	NCBI36
NG_007484.2:g.6414T>A , LRG_490:g.6414T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000257904.11:c.477T>A MANE Select	ENSP00000257904.5:p.Phe159Leu
ENST00000257904.10:c.477T>A	ENSP00000257904.5:p.Phe159Leu
ENST00000312990.10:c.265-297T>A	ENSP00000316889.6:n.265-297T>A
ENST00000546489.5:c.255T>A	ENSP00000447779.1:p.Phe85Leu
ENST00000547281.5:c.255T>A	ENSP00000447274.1:p.Phe85Leu
ENST00000549606.5:c.-158+1207T>A	ENSP00000447005.1:n.-158+1207T>A
ENST00000550419.5:c.477T>A	ENSP00000448098.1:p.Phe159Leu
ENST00000551706.1:n.843T>A
ENST00000551800.5:c.255T>A	ENSP00000449391.1:p.Phe85Leu
ENST00000551888.5:n.443-297T>A
ENST00000552254.5:c.477T>A	ENSP00000449179.1:p.Phe159Leu
ENST00000552388.1:c.477T>A	ENSP00000448963.1:p.Phe159Leu
ENST00000553237.5:c.*116T>A	ENSP00000448885.1:n.*116T>A
NM_000075.3:c.477T>A	NP_000066.1:p.Phe159Leu
NM_000075.4:c.477T>A MANE Select	NP_000066.1:p.Phe159Leu