Canonical Allele Identifier: CA126965057

Gene: MEGF10

Linked Data

• dbSNP Id: rs906716944
• gnomAD v3: 5-127442887-A-G
• gnomAD v4: 5-127442887-A-G
• MyVariant Identifiers: chr5:g.126778579A>G (hg19) ; chr5:g.127442887A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127442887A>G , CM000667.2:g.127442887A>G	GRCh38
NC_000005.9:g.126778579A>G , CM000667.1:g.126778579A>G	GRCh37
NC_000005.8:g.126806478A>G	NCBI36
NG_032072.1:g.157124A>G
NG_032072.2:g.157124A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503335.7:c.2363-111A>G MANE Select	ENSP00000423354.2:n.2363-111A>G
ENST00000274473.6:c.2363-111A>G	ENSP00000274473.6:n.2363-111A>G
ENST00000503335.6:c.2363-111A>G	ENSP00000423354.2:n.2363-111A>G
NM_001256545.1:c.2363-111A>G	NP_001243474.1:n.2363-111A>G
NM_032446.2:c.2363-111A>G	NP_115822.1:n.2363-111A>G
XM_011543692.1:c.2363-111A>G	XP_011541994.1:n.2363-111A>G
XM_011543693.1:c.2363-111A>G	XP_011541995.1:n.2363-111A>G
XM_011543694.1:c.2363-111A>G	XP_011541996.1:n.2363-111A>G
XM_017009987.1:c.2528-111A>G	XP_016865476.1:n.2528-111A>G
XM_017009988.1:c.1223-111A>G	XP_016865477.1:n.1223-111A>G
NM_001256545.2:c.2363-111A>G MANE Select	NP_001243474.1:n.2363-111A>G
NM_032446.3:c.2363-111A>G	NP_115822.1:n.2363-111A>G