Canonical Allele Identifier: CA2360861657

Gene: E2F1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33675512_33675514delinsCTT , CM000682.2:g.33675512_33675514delinsCTT	GRCh38
NC_000020.10:g.32263318_32263320delinsCTT , CM000682.1:g.32263318_32263320delinsCTT	GRCh37
NC_000020.9:g.31726979_31726981delinsCTT	NCBI36
NG_046988.1:g.15891_15893delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343380.6:c.*1218_*1220delinsAAG MANE Select	ENSP00000345571.5:n.*1218_*1220delinsAAG
NM_005225.2:c.*1218_*1220delinsAAG	NP_005216.1:n.*1218_*1220delinsAAG
NM_005225.3:c.*1218_*1220delinsAAG MANE Select	NP_005216.1:n.*1218_*1220delinsAAG