Canonical Allele Identifier: CA1580859309

Gene: MEGF10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127442800C= , CM000667.2:g.127442800C=	GRCh38
NC_000005.9:g.126778492C= , CM000667.1:g.126778492C=	GRCh37
NC_000005.8:g.126806391C=	NCBI36
NG_032072.1:g.157037C=
NG_032072.2:g.157037C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503335.7:c.2363-198C= MANE Select	ENSP00000423354.2:n.2363-198C=
ENST00000274473.6:c.2363-198C=	ENSP00000274473.6:n.2363-198C=
ENST00000503335.6:c.2363-198C=	ENSP00000423354.2:n.2363-198C=
NM_001256545.1:c.2363-198C=	NP_001243474.1:n.2363-198C=
NM_032446.2:c.2363-198C=	NP_115822.1:n.2363-198C=
XM_011543692.1:c.2363-198C=	XP_011541994.1:n.2363-198C=
XM_011543693.1:c.2363-198C=	XP_011541995.1:n.2363-198C=
XM_011543694.1:c.2363-198C=	XP_011541996.1:n.2363-198C=
XM_017009987.1:c.2528-198C=	XP_016865476.1:n.2528-198C=
XM_017009988.1:c.1223-198C=	XP_016865477.1:n.1223-198C=
NM_001256545.2:c.2363-198C= MANE Select	NP_001243474.1:n.2363-198C=
NM_032446.3:c.2363-198C=	NP_115822.1:n.2363-198C=