Canonical Allele Identifier: CA2038994808
Gene: CDK4 HGNC NCBI

Linked Data

dbSNP Id: rs1955224093
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57750565_57750566del , CM000674.2:g.57750565_57750566del GRCh38
NC_000012.11:g.58144348_58144349del , CM000674.1:g.58144348_58144349del GRCh37
NC_000012.10:g.56430615_56430616del NCBI36
NG_007484.2:g.6818_6819del , LRG_490:g.6818_6819del

Transcript Alleles

HGVS Amino-acid change
ENST00000257904.11:c.632+92_632+93del MANE Select ENSP00000257904.5:n.632+92_632+93del
ENST00000257904.10:c.632+92_632+93del ENSP00000257904.5:n.632+92_632+93del
ENST00000312990.10:c.280+92_280+93del ENSP00000316889.6:n.280+92_280+93del
ENST00000546489.5:c.410+92_410+93del ENSP00000447779.1:n.410+92_410+93del
ENST00000547281.5:c.410+92_410+93del ENSP00000447274.1:n.410+92_410+93del
ENST00000549606.5:c.-157-1060_-157-1059del ENSP00000447005.1:n.-157-1060_-157-1059de...
ENST00000550419.5:c.523-1_523del
ENST00000551888.5:n.458+92_458+93del
ENST00000553237.5:c.*271+92_*271+93del ENSP00000448885.1:n.*271+92_*271+93del
NM_000075.3:c.632+92_632+93del NP_000066.1:n.632+92_632+93del
NM_000075.4:c.632+92_632+93del MANE Select NP_000066.1:n.632+92_632+93del
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