Canonical Allele Identifier: CA1580843017

Gene: MEGF10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127420077C= , CM000667.2:g.127420077C=	GRCh38
NC_000005.9:g.126755769C= , CM000667.1:g.126755769C=	GRCh37
NC_000005.8:g.126783668C=	NCBI36
NG_032072.1:g.134314C=
NG_032072.2:g.134314C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503335.7:c.1460C= MANE Select	ENSP00000423354.2:p.Pro487=
ENST00000274473.6:c.1460C=	ENSP00000274473.6:p.Pro487=
ENST00000418761.6:c.1460C=	ENSP00000416284.2:p.Pro487=
ENST00000503335.6:c.1460C=	ENSP00000423354.2:p.Pro487=
ENST00000508365.5:c.1460C=	ENSP00000423195.1:p.Pro487=
NM_001256545.1:c.1460C=	NP_001243474.1:p.Pro487=
NM_001308119.1:c.1460C=	NP_001295048.1:p.Pro487=
NM_001308121.1:c.1460C=	NP_001295050.1:p.Pro487=
NM_032446.2:c.1460C=	NP_115822.1:p.Pro487=
XM_011543692.1:c.1460C=	XP_011541994.1:p.Pro487=
XM_011543693.1:c.1460C=	XP_011541995.1:p.Pro487=
XM_011543694.1:c.1460C=	XP_011541996.1:p.Pro487=
XM_017009987.1:c.1625C=	XP_016865476.1:p.Pro542=
XM_017009988.1:c.320C=	XP_016865477.1:p.Pro107=
NM_001256545.2:c.1460C= MANE Select	NP_001243474.1:p.Pro487=
NM_032446.3:c.1460C=	NP_115822.1:p.Pro487=
NM_001308119.2:c.1460C=	NP_001295048.1:p.Pro487=
NM_001308121.2:c.1460C=	NP_001295050.1:p.Pro487=