Canonical Allele Identifier: CA1580859286
Gene: MEGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1765801506

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.127442742_127442743insGCAGCTGAAAG , CM000667.2:g.127442742_127442743insGCAGCTGAAAG GRCh38
NC_000005.9:g.126778434_126778435insGCAGCTGAAAG , CM000667.1:g.126778434_126778435insGCAGCTGAAAG GRCh37
NC_000005.8:g.126806333_126806334insGCAGCTGAAAG NCBI36
NG_032072.1:g.156979_156980insGCAGCTGAAAG
NG_032072.2:g.156979_156980insGCAGCTGAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000503335.7:c.2363-256_2363-255insGCAGCTGAAAG MANE Select ENSP00000423354.2:n.2363-256_2363-255insGCAGCTGAAAG
ENST00000274473.6:c.2363-256_2363-255insGCAGCTGAAAG ENSP00000274473.6:n.2363-256_2363-255insGCAGCTGAAAG
ENST00000503335.6:c.2363-256_2363-255insGCAGCTGAAAG ENSP00000423354.2:n.2363-256_2363-255insGCAGCTGAAAG
NM_001256545.1:c.2363-256_2363-255insGCAGCTGAAAG NP_001243474.1:n.2363-256_2363-255insGCAGCTGAAAG
NM_032446.2:c.2363-256_2363-255insGCAGCTGAAAG NP_115822.1:n.2363-256_2363-255insGCAGCTGAAAG
XM_011543692.1:c.2363-256_2363-255insGCAGCTGAAAG XP_011541994.1:n.2363-256_2363-255insGCAGCTGAAAG
XM_011543693.1:c.2363-256_2363-255insGCAGCTGAAAG XP_011541995.1:n.2363-256_2363-255insGCAGCTGAAAG
XM_011543694.1:c.2363-256_2363-255insGCAGCTGAAAG XP_011541996.1:n.2363-256_2363-255insGCAGCTGAAAG
XM_017009987.1:c.2528-256_2528-255insGCAGCTGAAAG XP_016865476.1:n.2528-256_2528-255insGCAGCTGAAAG
XM_017009988.1:c.1223-256_1223-255insGCAGCTGAAAG XP_016865477.1:n.1223-256_1223-255insGCAGCTGAAAG
NM_001256545.2:c.2363-256_2363-255insGCAGCTGAAAG MANE Select NP_001243474.1:n.2363-256_2363-255insGCAGCTGAAAG
NM_032446.3:c.2363-256_2363-255insGCAGCTGAAAG NP_115822.1:n.2363-256_2363-255insGCAGCTGAAAG