Canonical Allele Identifier: CA2619494384

Gene: CDK4

Linked Data

• gnomAD v4: 12-57750458-TTGGGAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57750459_57750464del , CM000674.2:g.57750459_57750464del	GRCh38
NC_000012.11:g.58144242_58144247del , CM000674.1:g.58144242_58144247del	GRCh37
NC_000012.10:g.56430509_56430514del	NCBI36
NG_007484.2:g.6918_6923del , LRG_490:g.6918_6923del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257904.11:c.632+192_632+197del MANE Select	ENSP00000257904.5:n.632+192_632+197del
ENST00000257904.10:c.632+192_632+197del	ENSP00000257904.5:n.632+192_632+197del
ENST00000312990.10:c.280+192_280+197del	ENSP00000316889.6:n.280+192_280+197del
ENST00000546489.5:c.410+192_410+197del	ENSP00000447779.1:n.410+192_410+197del
ENST00000547281.5:c.410+192_410+197del	ENSP00000447274.1:n.410+192_410+197del
ENST00000549606.5:c.-157-960_-157-955del	ENSP00000447005.1:n.-157-960_-157-955del
ENST00000550419.5:c.*16_*21del	ENSP00000448098.1:n.*16_*21del
ENST00000551888.5:n.458+192_458+197del
ENST00000553237.5:c.*271+192_*271+197del	ENSP00000448885.1:n.*271+192_*271+197del
NM_000075.3:c.632+192_632+197del	NP_000066.1:n.632+192_632+197del
NM_000075.4:c.632+192_632+197del MANE Select	NP_000066.1:n.632+192_632+197del