Canonical Allele Identifier: CA2018373822

Gene: EPS8

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.15777871T= , CM000674.2:g.15777871T=	GRCh38
NC_000012.11:g.15930805T= , CM000674.1:g.15930805T=	GRCh37
NC_000012.10:g.15822072T=	NCBI36
NG_041808.1:g.16706A=

Transcript Alleles

HGVS	Amino-acid Change
NM_004447.6:c.-22+11290A= MANE Select	NP_004438.3:n.-22+11290A=
ENST00000281172.10:c.-22+11290A= MANE Select	ENSP00000281172.5:n.-22+11290A=
NM_004447.5:c.-22+11290A=	NP_004438.3:n.-22+11290A=
ENST00000281172.9:c.-22+11290A=	ENSP00000281172.5:n.-22+11290A=
ENST00000535752.5:c.-21-94899A=	ENSP00000440591.1:n.-21-94899A=
ENST00000536793.5:c.-128+11290A=	ENSP00000438668.1:n.-128+11290A=
ENST00000536956.5:c.-22+11290A=	ENSP00000442883.1:n.-22+11290A=
ENST00000543363.5:c.-22+2708A=	ENSP00000444613.1:n.-22+2708A=
ENST00000543468.5:c.-22+11290A=	ENSP00000445985.1:n.-22+11290A=
ENST00000543523.5:c.-22+10092A=	ENSP00000441867.1:n.-22+10092A=
ENST00000544064.1:c.-156+11290A=	ENSP00000445815.1:n.-156+11290A=
ENST00000642278.1:c.-1352+11290A=	ENSP00000494689.1:n.-1352+11290A=
ENST00000642939.1:c.-82+11290A=	ENSP00000495312.1:n.-82+11290A=
ENST00000644374.1:c.-22+11290A=	ENSP00000495956.1:n.-22+11290A=
ENST00000645775.1:c.-82+11290A=	ENSP00000495824.1:n.-82+11290A=
ENST00000646123.1:c.-22+11290A=	ENSP00000494338.1:n.-22+11290A=
ENST00000646828.1:c.-82+35691A=	ENSP00000494842.1:n.-82+35691A=
ENST00000646918.1:c.-22+50310A=	ENSP00000495722.1:n.-22+50310A=
ENST00000647087.1:c.-22+59702A=	ENSP00000496406.1:n.-22+59702A=
ENST00000647224.1:c.-22+11290A=	ENSP00000496516.1:n.-22+11290A=
XM_011520605.1:c.-22+11290A=	XP_011518907.1:n.-22+11290A=
XM_011520605.3:c.-22+11290A=	XP_011518907.1:n.-22+11290A=
XM_024448882.1:c.-22+11132A=	XP_024304650.1:n.-22+11132A=