Canonical Allele Identifier: CA683260

Gene: E2F2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23516486G>A , CM000663.2:g.23516486G>A	GRCh38
NC_000001.10:g.23842978G>A , CM000663.1:g.23842978G>A	GRCh37
NC_000001.9:g.23715565G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361729.3:c.894C>T MANE Select	ENSP00000355249.2:p.Ile298=
ENST00000361729.2:c.894C>T	ENSP00000355249.2:p.Ile298=
ENST00000487237.1:n.423C>T
NM_004091.3:c.894C>T	NP_004082.1:p.Ile298=
XM_005245748.2:c.330C>T	XP_005245805.1:p.Ile110=
XM_005245749.2:c.306C>T	XP_005245806.1:p.Ile102=
XM_011540868.1:c.888C>T	XP_011539170.1:p.Ile296=
XM_011540869.1:c.894C>T	XP_011539171.1:p.Ile298=
XM_011540870.1:c.894C>T	XP_011539172.1:p.Ile298=
XM_011540871.1:c.306C>T	XP_011539173.1:p.Ile102=
XM_005245748.3:c.330C>T	XP_005245805.1:p.Ile110=
XM_005245749.3:c.306C>T	XP_005245806.1:p.Ile102=
XM_011540868.3:c.888C>T	XP_011539170.1:p.Ile296=
XM_011540870.3:c.894C>T	XP_011539172.1:p.Ile298=
XM_011540871.2:c.306C>T	XP_011539173.1:p.Ile102=
NM_004091.4:c.894C>T MANE Select	NP_004082.1:p.Ile298=