Canonical Allele Identifier: CA385546410

Gene: CDK4

Linked Data

• dbSNP Id: rs763429253
• MyVariant Identifiers: chr12:g.58144773C>A (hg19) ; chr12:g.57750990C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750990C>A , CM000674.2:g.57750990C>A	GRCh38
NC_000012.11:g.58144773C>A , CM000674.1:g.58144773C>A	GRCh37
NC_000012.10:g.56431040C>A	NCBI36
NG_007484.2:g.6392G>T , LRG_490:g.6392G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000257904.11:c.455G>T MANE Select	ENSP00000257904.5:p.Gly152Val
ENST00000257904.10:c.455G>T	ENSP00000257904.5:p.Gly152Val
ENST00000312990.10:c.264+307G>T	ENSP00000316889.6:n.264+307G>T
ENST00000546489.5:c.233G>T	ENSP00000447779.1:p.Gly78Val
ENST00000547281.5:c.233G>T	ENSP00000447274.1:p.Gly78Val
ENST00000549606.5:c.-158+1185G>T	ENSP00000447005.1:n.-158+1185G>T
ENST00000550419.5:c.455G>T	ENSP00000448098.1:p.Gly152Val
ENST00000551706.1:n.821G>T
ENST00000551800.5:c.233G>T	ENSP00000449391.1:p.Gly78Val
ENST00000551888.5:n.442+307G>T
ENST00000552254.5:c.455G>T	ENSP00000449179.1:p.Gly152Val
ENST00000552388.1:c.455G>T	ENSP00000448963.1:p.Gly152Val
ENST00000553237.5:c.*94G>T	ENSP00000448885.1:n.*94G>T
NM_000075.3:c.455G>T	NP_000066.1:p.Gly152Val
NM_000075.4:c.455G>T MANE Select	NP_000066.1:p.Gly152Val