Canonical Allele Identifier: CA416600945

Gene: E2F2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23519073T>C , CM000663.2:g.23519073T>C	GRCh38
NC_000001.10:g.23845565T>C , CM000663.1:g.23845565T>C	GRCh37
NC_000001.9:g.23718152T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004091.4:c.795A>G MANE Select	NP_004082.1:p.Thr265=
ENST00000361729.3:c.795A>G MANE Select	ENSP00000355249.2:p.Thr265=
NM_004091.3:c.795A>G	NP_004082.1:p.Thr265=
ENST00000361729.2:c.795A>G	ENSP00000355249.2:p.Thr265=
ENST00000487237.1:n.324A>G
XM_005245748.2:c.231A>G	XP_005245805.1:p.Thr77=
XM_005245748.3:c.231A>G	XP_005245805.1:p.Thr77=
XM_005245749.2:c.207A>G	XP_005245806.1:p.Thr69=
XM_005245749.3:c.207A>G	XP_005245806.1:p.Thr69=
XM_011540868.1:c.789A>G	XP_011539170.1:p.Thr263=
XM_011540868.3:c.789A>G	XP_011539170.1:p.Thr263=
XM_011540869.1:c.795A>G	XP_011539171.1:p.Thr265=
XM_011540870.1:c.795A>G	XP_011539172.1:p.Thr265=
XM_011540870.3:c.795A>G	XP_011539172.1:p.Thr265=
XM_011540871.1:c.207A>G	XP_011539173.1:p.Thr69=
XM_011540871.2:c.207A>G	XP_011539173.1:p.Thr69=