Canonical Allele Identifier: CA2619494467

Gene: CDK4

Linked Data

• gnomAD v4: 12-57750566-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750574_57750575dup , CM000674.2:g.57750574_57750575dup	GRCh38
NC_000012.11:g.58144357_58144358dup , CM000674.1:g.58144357_58144358dup	GRCh37
NC_000012.10:g.56430624_56430625dup	NCBI36
NG_007484.2:g.6814_6815dup , LRG_490:g.6814_6815dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.632+88_632+89dup MANE Select	ENSP00000257904.5:n.632+88_632+89dup
ENST00000257904.10:c.632+88_632+89dup	ENSP00000257904.5:n.632+88_632+89dup
ENST00000312990.10:c.280+88_280+89dup	ENSP00000316889.6:n.280+88_280+89dup
ENST00000546489.5:c.410+88_410+89dup	ENSP00000447779.1:n.410+88_410+89dup
ENST00000547281.5:c.410+88_410+89dup	ENSP00000447274.1:n.410+88_410+89dup
ENST00000549606.5:c.-157-1064_-157-1063dup	ENSP00000447005.1:n.-157-1064_-157-1063dup
ENST00000550419.5:c.523-5_523-4dup	ENSP00000448098.1:n.523-5_523-4dup
ENST00000551888.5:n.458+88_458+89dup
ENST00000553237.5:c.*271+88_*271+89dup	ENSP00000448885.1:n.*271+88_*271+89dup
NM_000075.3:c.632+88_632+89dup	NP_000066.1:n.632+88_632+89dup
NM_000075.4:c.632+88_632+89dup MANE Select	NP_000066.1:n.632+88_632+89dup