Canonical Allele Identifier: CA126927753

Gene: MEGF10

Linked Data

• dbSNP Id: rs17765
• MyVariant Identifiers: chr5:g.126729395T>G (hg19) ; chr5:g.127393703T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127393703T>G , CM000667.2:g.127393703T>G	GRCh38
NC_000005.9:g.126729395T>G , CM000667.1:g.126729395T>G	GRCh37
NC_000005.8:g.126757294T>G	NCBI36
NG_032072.1:g.107940T>G
NG_032072.2:g.107940T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503335.7:c.413-2829T>G MANE Select	ENSP00000423354.2:n.413-2829T>G
ENST00000274473.6:c.413-2829T>G	ENSP00000274473.6:n.413-2829T>G
ENST00000418761.6:c.413-2829T>G	ENSP00000416284.2:n.413-2829T>G
ENST00000503335.6:c.413-2829T>G	ENSP00000423354.2:n.413-2829T>G
ENST00000508365.5:c.413-2829T>G	ENSP00000423195.1:n.413-2829T>G
NM_001256545.1:c.413-2829T>G	NP_001243474.1:n.413-2829T>G
NM_001308119.1:c.413-2829T>G	NP_001295048.1:n.413-2829T>G
NM_001308121.1:c.413-2829T>G	NP_001295050.1:n.413-2829T>G
NM_032446.2:c.413-2829T>G	NP_115822.1:n.413-2829T>G
XM_011543692.1:c.413-2829T>G	XP_011541994.1:n.413-2829T>G
XM_011543693.1:c.413-2829T>G	XP_011541995.1:n.413-2829T>G
XM_011543694.1:c.413-2829T>G	XP_011541996.1:n.413-2829T>G
XM_017009987.1:c.578-2829T>G	XP_016865476.1:n.578-2829T>G
NM_001256545.2:c.413-2829T>G MANE Select	NP_001243474.1:n.413-2829T>G
NM_032446.3:c.413-2829T>G	NP_115822.1:n.413-2829T>G
NM_001308119.2:c.413-2829T>G	NP_001295048.1:n.413-2829T>G
NM_001308121.2:c.413-2829T>G	NP_001295050.1:n.413-2829T>G