Canonical Allele Identifier: CA1580859264
Gene: MEGF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.127442709_127442712delinsTCCA , CM000667.2:g.127442709_127442712delinsTCCA GRCh38
NC_000005.9:g.126778401_126778404delinsTCCA , CM000667.1:g.126778401_126778404delinsTCCA GRCh37
NC_000005.8:g.126806300_126806303delinsTCCA NCBI36
NG_032072.1:g.156946_156949delinsTCCA
NG_032072.2:g.156946_156949delinsTCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000503335.7:c.2363-289_2363-286delinsTCCA MANE Select ENSP00000423354.2:n.2363-289_2363-286delinsTCCA
ENST00000274473.6:c.2363-289_2363-286delinsTCCA ENSP00000274473.6:n.2363-289_2363-286delinsTCCA
ENST00000503335.6:c.2363-289_2363-286delinsTCCA ENSP00000423354.2:n.2363-289_2363-286delinsTCCA
NM_001256545.1:c.2363-289_2363-286delinsTCCA NP_001243474.1:n.2363-289_2363-286delinsTCCA
NM_032446.2:c.2363-289_2363-286delinsTCCA NP_115822.1:n.2363-289_2363-286delinsTCCA
XM_011543692.1:c.2363-289_2363-286delinsTCCA XP_011541994.1:n.2363-289_2363-286delinsTCCA
XM_011543693.1:c.2363-289_2363-286delinsTCCA XP_011541995.1:n.2363-289_2363-286delinsTCCA
XM_011543694.1:c.2363-289_2363-286delinsTCCA XP_011541996.1:n.2363-289_2363-286delinsTCCA
XM_017009987.1:c.2528-289_2528-286delinsTCCA XP_016865476.1:n.2528-289_2528-286delinsTCCA
XM_017009988.1:c.1223-289_1223-286delinsTCCA XP_016865477.1:n.1223-289_1223-286delinsTCCA
NM_001256545.2:c.2363-289_2363-286delinsTCCA MANE Select NP_001243474.1:n.2363-289_2363-286delinsTCCA
NM_032446.3:c.2363-289_2363-286delinsTCCA NP_115822.1:n.2363-289_2363-286delinsTCCA