Canonical Allele Identifier: CA920203459

Gene: E2F1

Linked Data

• dbSNP Id: rs1601183243

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33675515_33675516del , CM000682.2:g.33675515_33675516del	GRCh38
NC_000020.10:g.32263321_32263322del , CM000682.1:g.32263321_32263322del	GRCh37
NC_000020.9:g.31726982_31726983del	NCBI36
NG_046988.1:g.15891_15892del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343380.6:c.*1218_*1219del MANE Select	ENSP00000345571.5:n.*1218_*1219del
NM_005225.2:c.*1218_*1219del	NP_005216.1:n.*1218_*1219del
NM_005225.3:c.*1218_*1219del MANE Select	NP_005216.1:n.*1218_*1219del