Canonical Allele Identifier: CA917577574

Gene: MEGF10

Linked Data

• dbSNP Id: rs1580876361

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127442699_127442700del , CM000667.2:g.127442699_127442700del	GRCh38
NC_000005.9:g.126778391_126778392del , CM000667.1:g.126778391_126778392del	GRCh37
NC_000005.8:g.126806290_126806291del	NCBI36
NG_032072.1:g.156936_156937del
NG_032072.2:g.156936_156937del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503335.7:c.2363-299_2363-298del MANE Select	ENSP00000423354.2:n.2363-299_2363-298del
ENST00000274473.6:c.2363-299_2363-298del	ENSP00000274473.6:n.2363-299_2363-298del
ENST00000503335.6:c.2363-299_2363-298del	ENSP00000423354.2:n.2363-299_2363-298del
NM_001256545.1:c.2363-299_2363-298del	NP_001243474.1:n.2363-299_2363-298del
NM_032446.2:c.2363-299_2363-298del	NP_115822.1:n.2363-299_2363-298del
XM_011543692.1:c.2363-299_2363-298del	XP_011541994.1:n.2363-299_2363-298del
XM_011543693.1:c.2363-299_2363-298del	XP_011541995.1:n.2363-299_2363-298del
XM_011543694.1:c.2363-299_2363-298del	XP_011541996.1:n.2363-299_2363-298del
XM_017009987.1:c.2528-299_2528-298del	XP_016865476.1:n.2528-299_2528-298del
XM_017009988.1:c.1223-299_1223-298del	XP_016865477.1:n.1223-299_1223-298del
NM_001256545.2:c.2363-299_2363-298del MANE Select	NP_001243474.1:n.2363-299_2363-298del
NM_032446.3:c.2363-299_2363-298del	NP_115822.1:n.2363-299_2363-298del