Canonical Allele Identifier: CA2038994651

Gene: CDK4

Linked Data

• dbSNP Id: rs769892118
• gnomAD v4: 12-57750498-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750498T>G , CM000674.2:g.57750498T>G	GRCh38
NC_000012.11:g.58144281T>G , CM000674.1:g.58144281T>G	GRCh37
NC_000012.10:g.56430548T>G	NCBI36
NG_007484.2:g.6884A>C , LRG_490:g.6884A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.632+158A>C MANE Select	ENSP00000257904.5:n.632+158A>C
ENST00000257904.10:c.632+158A>C	ENSP00000257904.5:n.632+158A>C
ENST00000312990.10:c.280+158A>C	ENSP00000316889.6:n.280+158A>C
ENST00000546489.5:c.410+158A>C	ENSP00000447779.1:n.410+158A>C
ENST00000547281.5:c.410+158A>C	ENSP00000447274.1:n.410+158A>C
ENST00000549606.5:c.-157-994A>C	ENSP00000447005.1:n.-157-994A>C
ENST00000550419.5:c.588A>C	ENSP00000448098.1:p.Gln196His
ENST00000551888.5:n.458+158A>C
ENST00000553237.5:c.*271+158A>C	ENSP00000448885.1:n.*271+158A>C
NM_000075.3:c.632+158A>C	NP_000066.1:n.632+158A>C
NM_000075.4:c.632+158A>C MANE Select	NP_000066.1:n.632+158A>C