Canonical Allele Identifier: CA385549110

Gene: CDK4

Linked Data

• ClinVar Variation Id: 463468
• ClinVar RCV Id: RCV000527911 ; RCV002341313 ; RCV003153698
• dbSNP Id: rs1555201383
• gnomAD v4: 12-57751669-A-G
• MyVariant Identifiers: chr12:g.58145452A>G (hg19) ; chr12:g.57751669A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57751669A>G , CM000674.2:g.57751669A>G	GRCh38
NC_000012.11:g.58145452A>G , CM000674.1:g.58145452A>G	GRCh37
NC_000012.10:g.56431719A>G	NCBI36
NG_007484.2:g.5713T>C , LRG_490:g.5713T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.49T>C MANE Select	ENSP00000257904.5:p.Tyr17His
ENST00000257904.10:c.49T>C	ENSP00000257904.5:p.Tyr17His
ENST00000312990.10:c.49T>C	ENSP00000316889.6:p.Tyr17His
ENST00000546489.5:c.-4-327T>C	ENSP00000447779.1:n.-4-327T>C
ENST00000547281.5:c.-164-10T>C	ENSP00000447274.1:n.-164-10T>C
ENST00000549606.5:c.-158+506T>C	ENSP00000447005.1:n.-158+506T>C
ENST00000550419.5:c.49T>C	ENSP00000448098.1:p.Tyr17His
ENST00000551706.1:n.258T>C
ENST00000551800.5:c.-174T>C	ENSP00000449391.1:n.-174T>C
ENST00000551888.5:n.227T>C
ENST00000552254.5:c.49T>C	ENSP00000449179.1:p.Tyr17His
ENST00000552388.1:c.49T>C	ENSP00000448963.1:p.Tyr17His
ENST00000552862.1:c.49T>C	ENSP00000446763.1:p.Tyr17His
ENST00000553237.5:c.49T>C	ENSP00000448885.1:p.Tyr17His
NM_000075.3:c.49T>C	NP_000066.1:p.Tyr17His
NM_000075.4:c.49T>C MANE Select	NP_000066.1:p.Tyr17His