Canonical Allele Identifier: CA1580843015

Gene: MEGF10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127420074G= , CM000667.2:g.127420074G=	GRCh38
NC_000005.9:g.126755766G= , CM000667.1:g.126755766G=	GRCh37
NC_000005.8:g.126783665G=	NCBI36
NG_032072.1:g.134311G=
NG_032072.2:g.134311G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000503335.7:c.1457G= MANE Select	ENSP00000423354.2:p.Cys486=
ENST00000274473.6:c.1457G=	ENSP00000274473.6:p.Cys486=
ENST00000418761.6:c.1457G=	ENSP00000416284.2:p.Cys486=
ENST00000503335.6:c.1457G=	ENSP00000423354.2:p.Cys486=
ENST00000508365.5:c.1457G=	ENSP00000423195.1:p.Cys486=
NM_001256545.1:c.1457G=	NP_001243474.1:p.Cys486=
NM_001308119.1:c.1457G=	NP_001295048.1:p.Cys486=
NM_001308121.1:c.1457G=	NP_001295050.1:p.Cys486=
NM_032446.2:c.1457G=	NP_115822.1:p.Cys486=
XM_011543692.1:c.1457G=	XP_011541994.1:p.Cys486=
XM_011543693.1:c.1457G=	XP_011541995.1:p.Cys486=
XM_011543694.1:c.1457G=	XP_011541996.1:p.Cys486=
XM_017009987.1:c.1622G=	XP_016865476.1:p.Cys541=
XM_017009988.1:c.317G=	XP_016865477.1:p.Cys106=
NM_001256545.2:c.1457G= MANE Select	NP_001243474.1:p.Cys486=
NM_032446.3:c.1457G=	NP_115822.1:p.Cys486=
NM_001308119.2:c.1457G=	NP_001295048.1:p.Cys486=
NM_001308121.2:c.1457G=	NP_001295050.1:p.Cys486=