Canonical Allele Identifier: CA360734359
Community Standard Title: NM_001256545.2(MEGF10):c.2429G>A (p.Cys810Tyr)
Gene: MEGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.127443064G>A , CM000667.2:g.127443064G>A GRCh38
NC_000005.9:g.126778756G>A , CM000667.1:g.126778756G>A GRCh37
NC_000005.8:g.126806655G>A NCBI36
NG_032072.1:g.157301G>A
NG_032072.2:g.157301G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001256545.2:c.2429G>A MANE Select NP_001243474.1:p.Cys810Tyr
ENST00000503335.7:c.2429G>A MANE Select ENSP00000423354.2:p.Cys810Tyr
NM_001256545.1:c.2429G>A NP_001243474.1:p.Cys810Tyr
NM_032446.2:c.2429G>A NP_115822.1:p.Cys810Tyr
NM_032446.3:c.2429G>A NP_115822.1:p.Cys810Tyr
ENST00000274473.6:c.2429G>A ENSP00000274473.6:p.Cys810Tyr
ENST00000503335.6:c.2429G>A ENSP00000423354.2:p.Cys810Tyr
XM_011543692.1:c.2429G>A XP_011541994.1:p.Cys810Tyr
XM_011543693.1:c.2429G>A XP_011541995.1:p.Cys810Tyr
XM_011543694.1:c.2429G>A XP_011541996.1:p.Cys810Tyr
XM_017009987.1:c.2594G>A XP_016865476.1:p.Cys865Tyr
XM_017009988.1:c.1289G>A XP_016865477.1:p.Cys430Tyr