Canonical Allele Identifier: CA2360861675
Gene: E2F1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33675579C= , CM000682.2:g.33675579C= GRCh38
NC_000020.10:g.32263385C= , CM000682.1:g.32263385C= GRCh37
NC_000020.9:g.31727046C= NCBI36
NG_046988.1:g.15826G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343380.6:c.*1153G= MANE Select ENSP00000345571.5:n.*1153G=
NM_005225.2:c.*1153G= NP_005216.1:n.*1153G=
NM_005225.3:c.*1153G= MANE Select NP_005216.1:n.*1153G=
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