Canonical Allele Identifier: CA2842079968

Gene: MEGF10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127393733T>C , CM000667.2:g.127393733T>C	GRCh38
NC_000005.9:g.126729425T>C , CM000667.1:g.126729425T>C	GRCh37
NC_000005.8:g.126757324T>C	NCBI36
NG_032072.1:g.107970T>C
NG_032072.2:g.107970T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503335.7:c.413-2799T>C MANE Select	ENSP00000423354.2:n.413-2799T>C
ENST00000274473.6:c.413-2799T>C	ENSP00000274473.6:n.413-2799T>C
ENST00000418761.6:c.413-2799T>C	ENSP00000416284.2:n.413-2799T>C
ENST00000503335.6:c.413-2799T>C	ENSP00000423354.2:n.413-2799T>C
ENST00000508365.5:c.413-2799T>C	ENSP00000423195.1:n.413-2799T>C
NM_001256545.1:c.413-2799T>C	NP_001243474.1:n.413-2799T>C
NM_001308119.1:c.413-2799T>C	NP_001295048.1:n.413-2799T>C
NM_001308121.1:c.413-2799T>C	NP_001295050.1:n.413-2799T>C
NM_032446.2:c.413-2799T>C	NP_115822.1:n.413-2799T>C
XM_011543692.1:c.413-2799T>C	XP_011541994.1:n.413-2799T>C
XM_011543693.1:c.413-2799T>C	XP_011541995.1:n.413-2799T>C
XM_011543694.1:c.413-2799T>C	XP_011541996.1:n.413-2799T>C
XM_017009987.1:c.578-2799T>C	XP_016865476.1:n.578-2799T>C
NM_001256545.2:c.413-2799T>C MANE Select	NP_001243474.1:n.413-2799T>C
NM_032446.3:c.413-2799T>C	NP_115822.1:n.413-2799T>C
NM_001308119.2:c.413-2799T>C	NP_001295048.1:n.413-2799T>C
NM_001308121.2:c.413-2799T>C	NP_001295050.1:n.413-2799T>C