Canonical Allele Identifier: CA2360861679
Gene: E2F1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33675587_33675588delinsGA , CM000682.2:g.33675587_33675588delinsGA GRCh38
NC_000020.10:g.32263393_32263394delinsGA , CM000682.1:g.32263393_32263394delinsGA GRCh37
NC_000020.9:g.31727054_31727055delinsGA NCBI36
NG_046988.1:g.15817_15818delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000343380.6:c.*1144_*1145delinsTC MANE Select ENSP00000345571.5:n.*1144_*1145delinsTC
NM_005225.2:c.*1144_*1145delinsTC NP_005216.1:n.*1144_*1145delinsTC
NM_005225.3:c.*1144_*1145delinsTC MANE Select NP_005216.1:n.*1144_*1145delinsTC