Canonical Allele Identifier: CA385548804

Gene: CDK4

Linked Data

• dbSNP Id: rs761965434
• MyVariant Identifiers: chr12:g.58145383G>T (hg19) ; chr12:g.57751600G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57751600G>T , CM000674.2:g.57751600G>T	GRCh38
NC_000012.11:g.58145383G>T , CM000674.1:g.58145383G>T	GRCh37
NC_000012.10:g.56431650G>T	NCBI36
NG_007484.2:g.5782C>A , LRG_490:g.5782C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000257904.11:c.118C>A MANE Select	ENSP00000257904.5:p.Pro40Thr
ENST00000257904.10:c.118C>A	ENSP00000257904.5:p.Pro40Thr
ENST00000312990.10:c.118C>A	ENSP00000316889.6:p.Pro40Thr
ENST00000546489.5:c.-4-258C>A	ENSP00000447779.1:n.-4-258C>A
ENST00000547281.5:c.-105C>A	ENSP00000447274.1:n.-105C>A
ENST00000549606.5:c.-158+575C>A	ENSP00000447005.1:n.-158+575C>A
ENST00000550419.5:c.118C>A	ENSP00000448098.1:p.Pro40Thr
ENST00000551706.1:n.327C>A
ENST00000551800.5:c.-105C>A	ENSP00000449391.1:n.-105C>A
ENST00000551888.5:n.296C>A
ENST00000552254.5:c.118C>A	ENSP00000449179.1:p.Pro40Thr
ENST00000552388.1:c.118C>A	ENSP00000448963.1:p.Pro40Thr
ENST00000552862.1:c.118C>A	ENSP00000446763.1:p.Pro40Thr
ENST00000553237.5:c.118C>A	ENSP00000448885.1:p.Pro40Thr
NM_000075.3:c.118C>A	NP_000066.1:p.Pro40Thr
NM_000075.4:c.118C>A MANE Select	NP_000066.1:p.Pro40Thr