Canonical Allele Identifier: CA1580859253

Gene: MEGF10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127442698_127442700delinsTCC , CM000667.2:g.127442698_127442700delinsTCC	GRCh38
NC_000005.9:g.126778390_126778392delinsTCC , CM000667.1:g.126778390_126778392delinsTCC	GRCh37
NC_000005.8:g.126806289_126806291delinsTCC	NCBI36
NG_032072.1:g.156935_156937delinsTCC
NG_032072.2:g.156935_156937delinsTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503335.7:c.2363-300_2363-298delinsTCC MANE Select	ENSP00000423354.2:n.2363-300_2363-298delinsTCC
ENST00000274473.6:c.2363-300_2363-298delinsTCC	ENSP00000274473.6:n.2363-300_2363-298delinsTCC
ENST00000503335.6:c.2363-300_2363-298delinsTCC	ENSP00000423354.2:n.2363-300_2363-298delinsTCC
NM_001256545.1:c.2363-300_2363-298delinsTCC	NP_001243474.1:n.2363-300_2363-298delinsTCC
NM_032446.2:c.2363-300_2363-298delinsTCC	NP_115822.1:n.2363-300_2363-298delinsTCC
XM_011543692.1:c.2363-300_2363-298delinsTCC	XP_011541994.1:n.2363-300_2363-298delinsTCC
XM_011543693.1:c.2363-300_2363-298delinsTCC	XP_011541995.1:n.2363-300_2363-298delinsTCC
XM_011543694.1:c.2363-300_2363-298delinsTCC	XP_011541996.1:n.2363-300_2363-298delinsTCC
XM_017009987.1:c.2528-300_2528-298delinsTCC	XP_016865476.1:n.2528-300_2528-298delinsTCC
XM_017009988.1:c.1223-300_1223-298delinsTCC	XP_016865477.1:n.1223-300_1223-298delinsTCC
NM_001256545.2:c.2363-300_2363-298delinsTCC MANE Select	NP_001243474.1:n.2363-300_2363-298delinsTCC
NM_032446.3:c.2363-300_2363-298delinsTCC	NP_115822.1:n.2363-300_2363-298delinsTCC