Canonical Allele Identifier: CA360822119

Gene: MEGF10

Linked Data

• MyVariant Identifiers: chr5:g.126674871G>A (hg19) ; chr5:g.127339179G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127339179G>A , CM000667.2:g.127339179G>A	GRCh38
NC_000005.9:g.126674871G>A , CM000667.1:g.126674871G>A	GRCh37
NC_000005.8:g.126702770G>A	NCBI36
NG_032072.1:g.53416G>A
NG_032072.2:g.53416G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503335.7:c.176G>A MANE Select	ENSP00000423354.2:p.Ser59Asn
ENST00000274473.6:c.176G>A	ENSP00000274473.6:p.Ser59Asn
ENST00000418761.6:c.176G>A	ENSP00000416284.2:p.Ser59Asn
ENST00000503335.6:c.176G>A	ENSP00000423354.2:p.Ser59Asn
ENST00000508365.5:c.176G>A	ENSP00000423195.1:p.Ser59Asn
NM_001256545.1:c.176G>A	NP_001243474.1:p.Ser59Asn
NM_001308119.1:c.176G>A	NP_001295048.1:p.Ser59Asn
NM_001308121.1:c.176G>A	NP_001295050.1:p.Ser59Asn
NM_032446.2:c.176G>A	NP_115822.1:p.Ser59Asn
XM_011543692.1:c.176G>A	XP_011541994.1:p.Ser59Asn
XM_011543693.1:c.176G>A	XP_011541995.1:p.Ser59Asn
XM_011543694.1:c.176G>A	XP_011541996.1:p.Ser59Asn
XM_017009987.1:c.341G>A	XP_016865476.1:p.Ser114Asn
NM_001256545.2:c.176G>A MANE Select	NP_001243474.1:p.Ser59Asn
NM_032446.3:c.176G>A	NP_115822.1:p.Ser59Asn
NM_001308119.2:c.176G>A	NP_001295048.1:p.Ser59Asn
NM_001308121.2:c.176G>A	NP_001295050.1:p.Ser59Asn