Canonical Allele Identifier: CA360729825

Gene: MEGF10

Linked Data

• dbSNP Id: rs200050342
• COSMIC: COSM5642111
• MyVariant Identifiers: chr5:g.126755743C>A (hg19) ; chr5:g.127420051C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127420051C>A , CM000667.2:g.127420051C>A	GRCh38
NC_000005.9:g.126755743C>A , CM000667.1:g.126755743C>A	GRCh37
NC_000005.8:g.126783642C>A	NCBI36
NG_032072.1:g.134288C>A
NG_032072.2:g.134288C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503335.7:c.1434C>A MANE Select	ENSP00000423354.2:p.His478Gln
ENST00000274473.6:c.1434C>A	ENSP00000274473.6:p.His478Gln
ENST00000418761.6:c.1434C>A	ENSP00000416284.2:p.His478Gln
ENST00000503335.6:c.1434C>A	ENSP00000423354.2:p.His478Gln
ENST00000508365.5:c.1434C>A	ENSP00000423195.1:p.His478Gln
NM_001256545.1:c.1434C>A	NP_001243474.1:p.His478Gln
NM_001308119.1:c.1434C>A	NP_001295048.1:p.His478Gln
NM_001308121.1:c.1434C>A	NP_001295050.1:p.His478Gln
NM_032446.2:c.1434C>A	NP_115822.1:p.His478Gln
XM_011543692.1:c.1434C>A	XP_011541994.1:p.His478Gln
XM_011543693.1:c.1434C>A	XP_011541995.1:p.His478Gln
XM_011543694.1:c.1434C>A	XP_011541996.1:p.His478Gln
XM_017009987.1:c.1599C>A	XP_016865476.1:p.His533Gln
XM_017009988.1:c.294C>A	XP_016865477.1:p.His98Gln
NM_001256545.2:c.1434C>A MANE Select	NP_001243474.1:p.His478Gln
NM_032446.3:c.1434C>A	NP_115822.1:p.His478Gln
NM_001308119.2:c.1434C>A	NP_001295048.1:p.His478Gln
NM_001308121.2:c.1434C>A	NP_001295050.1:p.His478Gln