Canonical Allele Identifier: CA360730006

Gene: MEGF10

Linked Data

• gnomAD v4: 5-127420134-C-A
• MyVariant Identifiers: chr5:g.126755826C>A (hg19) ; chr5:g.127420134C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127420134C>A , CM000667.2:g.127420134C>A	GRCh38
NC_000005.9:g.126755826C>A , CM000667.1:g.126755826C>A	GRCh37
NC_000005.8:g.126783725C>A	NCBI36
NG_032072.1:g.134371C>A
NG_032072.2:g.134371C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503335.7:c.1517C>A MANE Select	ENSP00000423354.2:p.Ala506Asp
ENST00000274473.6:c.1517C>A	ENSP00000274473.6:p.Ala506Asp
ENST00000418761.6:c.1517C>A	ENSP00000416284.2:p.Ala506Asp
ENST00000503335.6:c.1517C>A	ENSP00000423354.2:p.Ala506Asp
ENST00000508365.5:c.1517C>A	ENSP00000423195.1:p.Ala506Asp
NM_001256545.1:c.1517C>A	NP_001243474.1:p.Ala506Asp
NM_001308119.1:c.1517C>A	NP_001295048.1:p.Ala506Asp
NM_001308121.1:c.1517C>A	NP_001295050.1:p.Ala506Asp
NM_032446.2:c.1517C>A	NP_115822.1:p.Ala506Asp
XM_011543692.1:c.1517C>A	XP_011541994.1:p.Ala506Asp
XM_011543693.1:c.1517C>A	XP_011541995.1:p.Ala506Asp
XM_011543694.1:c.1517C>A	XP_011541996.1:p.Ala506Asp
XM_017009987.1:c.1682C>A	XP_016865476.1:p.Ala561Asp
XM_017009988.1:c.377C>A	XP_016865477.1:p.Ala126Asp
NM_001256545.2:c.1517C>A MANE Select	NP_001243474.1:p.Ala506Asp
NM_032446.3:c.1517C>A	NP_115822.1:p.Ala506Asp
NM_001308119.2:c.1517C>A	NP_001295048.1:p.Ala506Asp
NM_001308121.2:c.1517C>A	NP_001295050.1:p.Ala506Asp