Canonical Allele Identifier: CA2675088450

Gene: MEGF10

Linked Data

• gnomAD v4: 5-127420280-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127420285del , CM000667.2:g.127420285del	GRCh38
NC_000005.9:g.126755977del , CM000667.1:g.126755977del	GRCh37
NC_000005.8:g.126783876del	NCBI36
NG_032072.1:g.134522del
NG_032072.2:g.134522del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503335.7:c.1590+78del MANE Select	ENSP00000423354.2:n.1590+78del
ENST00000274473.6:c.1590+78del	ENSP00000274473.6:n.1590+78del
ENST00000418761.6:c.1590+78del	ENSP00000416284.2:n.1590+78del
ENST00000503335.6:c.1590+78del	ENSP00000423354.2:n.1590+78del
ENST00000508365.5:c.1590+78del	ENSP00000423195.1:n.1590+78del
NM_001256545.1:c.1590+78del	NP_001243474.1:n.1590+78del
NM_001308119.1:c.1590+78del	NP_001295048.1:n.1590+78del
NM_001308121.1:c.1590+78del	NP_001295050.1:n.1590+78del
NM_032446.2:c.1590+78del	NP_115822.1:n.1590+78del
XM_011543692.1:c.1590+78del	XP_011541994.1:n.1590+78del
XM_011543693.1:c.1590+78del	XP_011541995.1:n.1590+78del
XM_011543694.1:c.1590+78del	XP_011541996.1:n.1590+78del
XM_017009987.1:c.1755+78del	XP_016865476.1:n.1755+78del
XM_017009988.1:c.450+78del	XP_016865477.1:n.450+78del
NM_001256545.2:c.1590+78del MANE Select	NP_001243474.1:n.1590+78del
NM_032446.3:c.1590+78del	NP_115822.1:n.1590+78del
NM_001308119.2:c.1590+78del	NP_001295048.1:n.1590+78del
NM_001308121.2:c.1590+78del	NP_001295050.1:n.1590+78del