Canonical Allele Identifier: CA2768314886

Gene: MEGF10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127442684_127442685dup , CM000667.2:g.127442684_127442685dup	GRCh38
NC_000005.9:g.126778376_126778377dup , CM000667.1:g.126778376_126778377dup	GRCh37
NC_000005.8:g.126806275_126806276dup	NCBI36
NG_032072.1:g.156921_156922dup
NG_032072.2:g.156921_156922dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503335.7:c.2363-314_2363-313dup MANE Select	ENSP00000423354.2:n.2363-314_2363-313dup
ENST00000274473.6:c.2363-314_2363-313dup	ENSP00000274473.6:n.2363-314_2363-313dup
ENST00000503335.6:c.2363-314_2363-313dup	ENSP00000423354.2:n.2363-314_2363-313dup
NM_001256545.1:c.2363-314_2363-313dup	NP_001243474.1:n.2363-314_2363-313dup
NM_032446.2:c.2363-314_2363-313dup	NP_115822.1:n.2363-314_2363-313dup
XM_011543692.1:c.2363-314_2363-313dup	XP_011541994.1:n.2363-314_2363-313dup
XM_011543693.1:c.2363-314_2363-313dup	XP_011541995.1:n.2363-314_2363-313dup
XM_011543694.1:c.2363-314_2363-313dup	XP_011541996.1:n.2363-314_2363-313dup
XM_017009987.1:c.2528-314_2528-313dup	XP_016865476.1:n.2528-314_2528-313dup
XM_017009988.1:c.1223-314_1223-313dup	XP_016865477.1:n.1223-314_1223-313dup
NM_001256545.2:c.2363-314_2363-313dup MANE Select	NP_001243474.1:n.2363-314_2363-313dup
NM_032446.3:c.2363-314_2363-313dup	NP_115822.1:n.2363-314_2363-313dup