Canonical Allele Identifier: CA2652499412
Gene: E2F1 HGNC NCBI

Linked Data

gnomAD v4: 20-33675512-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33675516del , CM000682.2:g.33675516del GRCh38
NC_000020.10:g.32263322del , CM000682.1:g.32263322del GRCh37
NC_000020.9:g.31726983del NCBI36
NG_046988.1:g.15892del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343380.6:c.*1219del MANE Select ENSP00000345571.5:n.*1219del
NM_005225.2:c.*1219del NP_005216.1:n.*1219del
NM_005225.3:c.*1219del MANE Select NP_005216.1:n.*1219del
Search 100 bp 5'
Search 100 bp 3'