Canonical Allele Identifier: CA2581093094

Gene: CDK4

Linked Data

• dbSNP Id: rs3211614

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57751138C>A , CM000674.2:g.57751138C>A	GRCh38
NC_000012.11:g.58144921C>A , CM000674.1:g.58144921C>A	GRCh37
NC_000012.10:g.56431188C>A	NCBI36
NG_007484.2:g.6244G>T , LRG_490:g.6244G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000257904.11:c.355-48G>T MANE Select	ENSP00000257904.5:n.355-48G>T
ENST00000257904.10:c.355-48G>T	ENSP00000257904.5:n.355-48G>T
ENST00000312990.10:c.264+159G>T	ENSP00000316889.6:n.264+159G>T
ENST00000546489.5:c.133-48G>T	ENSP00000447779.1:n.133-48G>T
ENST00000547281.5:c.133-48G>T	ENSP00000447274.1:n.133-48G>T
ENST00000549606.5:c.-158+1037G>T	ENSP00000447005.1:n.-158+1037G>T
ENST00000550419.5:c.355-48G>T	ENSP00000448098.1:n.355-48G>T
ENST00000551706.1:n.721-48G>T
ENST00000551800.5:c.133-48G>T	ENSP00000449391.1:n.133-48G>T
ENST00000551888.5:n.442+159G>T
ENST00000552254.5:c.355-48G>T	ENSP00000449179.1:n.355-48G>T
ENST00000552388.1:c.355-48G>T	ENSP00000448963.1:n.355-48G>T
ENST00000553237.5:c.219-48G>T	ENSP00000448885.1:n.219-48G>T
NM_000075.3:c.355-48G>T	NP_000066.1:n.355-48G>T
NM_000075.4:c.355-48G>T MANE Select	NP_000066.1:n.355-48G>T