Canonical Allele Identifier: CA2360861680
Gene: E2F1 HGNC NCBI

Linked Data

dbSNP Id: rs2017939289
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33675588del , CM000682.2:g.33675588del GRCh38
NC_000020.10:g.32263394del , CM000682.1:g.32263394del GRCh37
NC_000020.9:g.31727055del NCBI36
NG_046988.1:g.15817del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343380.6:c.*1144del MANE Select ENSP00000345571.5:n.*1144del
NM_005225.2:c.*1144del NP_005216.1:n.*1144del
NM_005225.3:c.*1144del MANE Select NP_005216.1:n.*1144del
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Search 100 bp 3'