Canonical Allele Identifier: CA1580842943
Gene: MEGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1764929311

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.127419989_127419991del , CM000667.2:g.127419989_127419991del GRCh38
NC_000005.9:g.126755681_126755683del , CM000667.1:g.126755681_126755683del GRCh37
NC_000005.8:g.126783580_126783582del NCBI36
NG_032072.1:g.134226_134228del
NG_032072.2:g.134226_134228del

Transcript Alleles

HGVS Amino-acid Change
ENST00000503335.7:c.1427-55_1427-53del MANE Select ENSP00000423354.2:n.1427-55_1427-53del
ENST00000274473.6:c.1427-55_1427-53del ENSP00000274473.6:n.1427-55_1427-53del
ENST00000418761.6:c.1427-55_1427-53del ENSP00000416284.2:n.1427-55_1427-53del
ENST00000503335.6:c.1427-55_1427-53del ENSP00000423354.2:n.1427-55_1427-53del
ENST00000508365.5:c.1427-55_1427-53del ENSP00000423195.1:n.1427-55_1427-53del
NM_001256545.1:c.1427-55_1427-53del NP_001243474.1:n.1427-55_1427-53del
NM_001308119.1:c.1427-55_1427-53del NP_001295048.1:n.1427-55_1427-53del
NM_001308121.1:c.1427-55_1427-53del NP_001295050.1:n.1427-55_1427-53del
NM_032446.2:c.1427-55_1427-53del NP_115822.1:n.1427-55_1427-53del
XM_011543692.1:c.1427-55_1427-53del XP_011541994.1:n.1427-55_1427-53del
XM_011543693.1:c.1427-55_1427-53del XP_011541995.1:n.1427-55_1427-53del
XM_011543694.1:c.1427-55_1427-53del XP_011541996.1:n.1427-55_1427-53del
XM_017009987.1:c.1592-55_1592-53del XP_016865476.1:n.1592-55_1592-53del
XM_017009988.1:c.287-55_287-53del XP_016865477.1:n.287-55_287-53del
NM_001256545.2:c.1427-55_1427-53del MANE Select NP_001243474.1:n.1427-55_1427-53del
NM_032446.3:c.1427-55_1427-53del NP_115822.1:n.1427-55_1427-53del
NM_001308119.2:c.1427-55_1427-53del NP_001295048.1:n.1427-55_1427-53del
NM_001308121.2:c.1427-55_1427-53del NP_001295050.1:n.1427-55_1427-53del