Canonical Allele Identifier: CA2038994688

Gene: CDK4

Linked Data

• dbSNP Id: rs1955223324

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750515T>C , CM000674.2:g.57750515T>C	GRCh38
NC_000012.11:g.58144298T>C , CM000674.1:g.58144298T>C	GRCh37
NC_000012.10:g.56430565T>C	NCBI36
NG_007484.2:g.6867A>G , LRG_490:g.6867A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.632+141A>G MANE Select	ENSP00000257904.5:n.632+141A>G
ENST00000257904.10:c.632+141A>G	ENSP00000257904.5:n.632+141A>G
ENST00000312990.10:c.280+141A>G	ENSP00000316889.6:n.280+141A>G
ENST00000546489.5:c.410+141A>G	ENSP00000447779.1:n.410+141A>G
ENST00000547281.5:c.410+141A>G	ENSP00000447274.1:n.410+141A>G
ENST00000549606.5:c.-157-1011A>G	ENSP00000447005.1:n.-157-1011A>G
ENST00000550419.5:c.571A>G	ENSP00000448098.1:p.Ser191Gly
ENST00000551888.5:n.458+141A>G
ENST00000553237.5:c.*271+141A>G	ENSP00000448885.1:n.*271+141A>G
NM_000075.3:c.632+141A>G	NP_000066.1:n.632+141A>G
NM_000075.4:c.632+141A>G MANE Select	NP_000066.1:n.632+141A>G