Canonical Allele Identifier: CA2360861648
Gene: E2F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33675488C= , CM000682.2:g.33675488C= GRCh38
NC_000020.10:g.32263294C= , CM000682.1:g.32263294C= GRCh37
NC_000020.9:g.31726955C= NCBI36
NG_046988.1:g.15917G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343380.6:c.*1244G= MANE Select ENSP00000345571.5:n.*1244G=
NM_005225.2:c.*1244G= NP_005216.1:n.*1244G=
NM_005225.3:c.*1244G= MANE Select NP_005216.1:n.*1244G=