Canonical Allele Identifier: CA917577575

Gene: MEGF10

Linked Data

• dbSNP Id: rs1580876382

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127442704_127442705insTGTT , CM000667.2:g.127442704_127442705insTGTT	GRCh38
NC_000005.9:g.126778396_126778397insTGTT , CM000667.1:g.126778396_126778397insTGTT	GRCh37
NC_000005.8:g.126806295_126806296insTGTT	NCBI36
NG_032072.1:g.156941_156942insTGTT
NG_032072.2:g.156941_156942insTGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503335.7:c.2363-294_2363-293insTGTT MANE Select	ENSP00000423354.2:n.2363-294_2363-293insTGTT
ENST00000274473.6:c.2363-294_2363-293insTGTT	ENSP00000274473.6:n.2363-294_2363-293insTGTT
ENST00000503335.6:c.2363-294_2363-293insTGTT	ENSP00000423354.2:n.2363-294_2363-293insTGTT
NM_001256545.1:c.2363-294_2363-293insTGTT	NP_001243474.1:n.2363-294_2363-293insTGTT
NM_032446.2:c.2363-294_2363-293insTGTT	NP_115822.1:n.2363-294_2363-293insTGTT
XM_011543692.1:c.2363-294_2363-293insTGTT	XP_011541994.1:n.2363-294_2363-293insTGTT
XM_011543693.1:c.2363-294_2363-293insTGTT	XP_011541995.1:n.2363-294_2363-293insTGTT
XM_011543694.1:c.2363-294_2363-293insTGTT	XP_011541996.1:n.2363-294_2363-293insTGTT
XM_017009987.1:c.2528-294_2528-293insTGTT	XP_016865476.1:n.2528-294_2528-293insTGTT
XM_017009988.1:c.1223-294_1223-293insTGTT	XP_016865477.1:n.1223-294_1223-293insTGTT
NM_001256545.2:c.2363-294_2363-293insTGTT MANE Select	NP_001243474.1:n.2363-294_2363-293insTGTT
NM_032446.3:c.2363-294_2363-293insTGTT	NP_115822.1:n.2363-294_2363-293insTGTT