Canonical Allele Identifier: CA2038997875

Gene: CDK4

Linked Data

• dbSNP Id: rs1955245171

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57752199G>C , CM000674.2:g.57752199G>C	GRCh38
NC_000012.11:g.58145982G>C , CM000674.1:g.58145982G>C	GRCh37
NC_000012.10:g.56432249G>C	NCBI36
NG_007484.2:g.5183C>G , LRG_490:g.5183C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000257904.11:c.-44C>G MANE Select	ENSP00000257904.5:n.-44C>G
ENST00000257904.10:c.-44C>G	ENSP00000257904.5:n.-44C>G
ENST00000312990.10:c.-44C>G	ENSP00000316889.6:n.-44C>G
ENST00000546489.5:c.-29C>G	ENSP00000447779.1:n.-29C>G
ENST00000547281.5:c.-189C>G	ENSP00000447274.1:n.-189C>G
ENST00000549606.5:c.-182C>G	ENSP00000447005.1:n.-182C>G
ENST00000550419.5:c.-44C>G	ENSP00000448098.1:n.-44C>G
ENST00000551706.1:n.166C>G
ENST00000551800.5:c.-226C>G	ENSP00000449391.1:n.-226C>G
ENST00000551888.5:n.135C>G
ENST00000552388.1:c.-60C>G	ENSP00000448963.1:n.-60C>G
ENST00000552862.1:c.-19-463C>G	ENSP00000446763.1:n.-19-463C>G
ENST00000553237.5:c.-44C>G	ENSP00000448885.1:n.-44C>G
NM_000075.3:c.-44C>G	NP_000066.1:n.-44C>G
NM_000075.4:c.-44C>G MANE Select	NP_000066.1:n.-44C>G