Canonical Allele Identifier: CA10620072

Gene: MEGF10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127460987C>A , CM000667.2:g.127460987C>A	GRCh38
NC_000005.9:g.126796679C>A , CM000667.1:g.126796679C>A	GRCh37
NC_000005.8:g.126824578C>A	NCBI36
NG_032072.1:g.175224C>A
NG_032072.2:g.175224C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503335.7:c.*3669C>A MANE Select	ENSP00000423354.2:n.*3669C>A
ENST00000274473.6:c.*3669C>A	ENSP00000274473.6:n.*3669C>A
ENST00000503335.6:c.*3669C>A	ENSP00000423354.2:n.*3669C>A
ENST00000515622.1:n.434-4619C>A
NM_001256545.1:c.*3669C>A	NP_001243474.1:n.*3669C>A
NM_032446.2:c.*3669C>A	NP_115822.1:n.*3669C>A
XM_011543692.1:c.*3669C>A	XP_011541994.1:n.*3669C>A
XM_011543693.1:c.*3669C>A	XP_011541995.1:n.*3669C>A
XM_011543694.1:c.*3669C>A	XP_011541996.1:n.*3669C>A
XM_017009987.1:c.*3669C>A	XP_016865476.1:n.*3669C>A
XM_017009988.1:c.*3669C>A	XP_016865477.1:n.*3669C>A
NM_001256545.2:c.*3669C>A MANE Select	NP_001243474.1:n.*3669C>A
NM_032446.3:c.*3669C>A	NP_115822.1:n.*3669C>A