Canonical Allele Identifier: CA2768314521
Gene: MEGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.127420115_127420116insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA , CM000667.2:g.127420115_127420116insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA GRCh38
NC_000005.9:g.126755807_126755808insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA , CM000667.1:g.126755807_126755808insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA GRCh37
NC_000005.8:g.126783706_126783707insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA NCBI36
NG_032072.1:g.134352_134353insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA
NG_032072.2:g.134352_134353insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000503335.7:c.1498_1499insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA MANE Select ENSP00000423354.2:p.Gln500ProfsTer5
ENST00000274473.6:c.1498_1499insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA ENSP00000274473.6:p.Gln500ProfsTer5
ENST00000418761.6:c.1498_1499insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA ENSP00000416284.2:p.Gln500ProfsTer5
ENST00000503335.6:c.1498_1499insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA ENSP00000423354.2:p.Gln500ProfsTer5
ENST00000508365.5:c.1498_1499insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA ENSP00000423195.1:p.Gln500ProfsTer5
NM_001256545.1:c.1498_1499insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA NP_001243474.1:p.Gln500ProfsTer5
NM_001308119.1:c.1498_1499insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA NP_001295048.1:p.Gln500ProfsTer5
NM_001308121.1:c.1498_1499insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA NP_001295050.1:p.Gln500ProfsTer5
NM_032446.2:c.1498_1499insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA NP_115822.1:p.Gln500ProfsTer5
XM_011543692.1:c.1498_1499insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA XP_011541994.1:p.Gln500ProfsTer5
XM_011543693.1:c.1498_1499insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA XP_011541995.1:p.Gln500ProfsTer5
XM_011543694.1:c.1498_1499insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA XP_011541996.1:p.Gln500ProfsTer5
XM_017009987.1:c.1663_1664insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA XP_016865476.1:p.Gln555ProfsTer5
XM_017009988.1:c.358_359insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA XP_016865477.1:p.Gln120ProfsTer5
NM_001256545.2:c.1498_1499insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA MANE Select NP_001243474.1:p.Gln500ProfsTer5
NM_032446.3:c.1498_1499insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA NP_115822.1:p.Gln500ProfsTer5
NM_001308119.2:c.1498_1499insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA NP_001295048.1:p.Gln500ProfsTer5
NM_001308121.2:c.1498_1499insCAAGGCGTTTCTAAAGAGAAACGTGGTTTGGAAAGGCTCAACA NP_001295050.1:p.Gln500ProfsTer5