Canonical Allele Identifier: CA2838186514

Gene: MEGF11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66159908T>G , CM000677.2:g.66159908T>G	GRCh38
NC_000015.9:g.66452246T>G , CM000677.1:g.66452246T>G	GRCh37
NC_000015.8:g.64239300T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001385028.1:c.-8-31497A>C MANE Select	NP_001371957.1:n.-8-31497A>C
ENST00000395614.6:c.-8-31497A>C MANE Select	ENSP00000378976.2:n.-8-31497A>C
NM_001385029.1:c.-8-31497A>C	NP_001371958.1:n.-8-31497A>C
NM_001385030.1:c.-26-35908A>C	NP_001371959.1:n.-26-35908A>C
NM_001385031.1:c.-142-35908A>C	NP_001371960.1:n.-142-35908A>C
NM_001385032.1:c.-142-35908A>C	NP_001371961.1:n.-142-35908A>C
NM_001385033.1:c.-8-31497A>C	NP_001371962.1:n.-8-31497A>C
NM_001387150.1:c.-30-31475A>C	NP_001374079.1:n.-30-31475A>C
NM_001387151.1:c.-8-31497A>C	NP_001374080.1:n.-8-31497A>C
NM_032445.2:c.-8-31497A>C	NP_115821.2:n.-8-31497A>C
NM_032445.3:c.-8-31497A>C	NP_115821.2:n.-8-31497A>C
NR_169554.1:n.147-35908A>C
NR_169555.1:n.147-35908A>C
NR_169556.1:n.147-31497A>C
NR_169557.1:n.147-31497A>C
NR_169558.1:n.147-31497A>C
ENST00000288745.7:c.-26-35908A>C	ENSP00000288745.3:n.-26-35908A>C
ENST00000409699.6:c.-30-31475A>C	ENSP00000386908.2:n.-30-31475A>C
ENST00000422354.5:c.-8-31497A>C	ENSP00000414475.1:n.-8-31497A>C
ENST00000422354.6:c.-8-31497A>C	ENSP00000414475.1:n.-8-31497A>C
XM_011522109.1:c.31+5418A>C	XP_011520411.1:n.31+5418A>C