Canonical Allele Identifier: CA1580859239

Gene: MEGF10

Linked Data

• dbSNP Id: rs1765798615
• gnomAD v3: 5-127442678-T-TGA
• gnomAD v4: 5-127442678-T-TGA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127442678_127442679insGA , CM000667.2:g.127442678_127442679insGA	GRCh38
NC_000005.9:g.126778370_126778371insGA , CM000667.1:g.126778370_126778371insGA	GRCh37
NC_000005.8:g.126806269_126806270insGA	NCBI36
NG_032072.1:g.156915_156916insGA
NG_032072.2:g.156915_156916insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503335.7:c.2363-320_2363-319insGA MANE Select	ENSP00000423354.2:n.2363-320_2363-319insGA
ENST00000274473.6:c.2363-320_2363-319insGA	ENSP00000274473.6:n.2363-320_2363-319insGA
ENST00000503335.6:c.2363-320_2363-319insGA	ENSP00000423354.2:n.2363-320_2363-319insGA
NM_001256545.1:c.2363-320_2363-319insGA	NP_001243474.1:n.2363-320_2363-319insGA
NM_032446.2:c.2363-320_2363-319insGA	NP_115822.1:n.2363-320_2363-319insGA
XM_011543692.1:c.2363-320_2363-319insGA	XP_011541994.1:n.2363-320_2363-319insGA
XM_011543693.1:c.2363-320_2363-319insGA	XP_011541995.1:n.2363-320_2363-319insGA
XM_011543694.1:c.2363-320_2363-319insGA	XP_011541996.1:n.2363-320_2363-319insGA
XM_017009987.1:c.2528-320_2528-319insGA	XP_016865476.1:n.2528-320_2528-319insGA
XM_017009988.1:c.1223-320_1223-319insGA	XP_016865477.1:n.1223-320_1223-319insGA
NM_001256545.2:c.2363-320_2363-319insGA MANE Select	NP_001243474.1:n.2363-320_2363-319insGA
NM_032446.3:c.2363-320_2363-319insGA	NP_115822.1:n.2363-320_2363-319insGA