Canonical Allele Identifier: CA360822416

Gene: MEGF10

Linked Data

• MyVariant Identifiers: chr5:g.126674895T>A (hg19) ; chr5:g.127339203T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127339203T>A , CM000667.2:g.127339203T>A	GRCh38
NC_000005.9:g.126674895T>A , CM000667.1:g.126674895T>A	GRCh37
NC_000005.8:g.126702794T>A	NCBI36
NG_032072.1:g.53440T>A
NG_032072.2:g.53440T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503335.7:c.200T>A MANE Select	ENSP00000423354.2:p.Phe67Tyr
ENST00000274473.6:c.200T>A	ENSP00000274473.6:p.Phe67Tyr
ENST00000418761.6:c.200T>A	ENSP00000416284.2:p.Phe67Tyr
ENST00000503335.6:c.200T>A	ENSP00000423354.2:p.Phe67Tyr
ENST00000508365.5:c.200T>A	ENSP00000423195.1:p.Phe67Tyr
NM_001256545.1:c.200T>A	NP_001243474.1:p.Phe67Tyr
NM_001308119.1:c.200T>A	NP_001295048.1:p.Phe67Tyr
NM_001308121.1:c.200T>A	NP_001295050.1:p.Phe67Tyr
NM_032446.2:c.200T>A	NP_115822.1:p.Phe67Tyr
XM_011543692.1:c.200T>A	XP_011541994.1:p.Phe67Tyr
XM_011543693.1:c.200T>A	XP_011541995.1:p.Phe67Tyr
XM_011543694.1:c.200T>A	XP_011541996.1:p.Phe67Tyr
XM_017009987.1:c.365T>A	XP_016865476.1:p.Phe122Tyr
NM_001256545.2:c.200T>A MANE Select	NP_001243474.1:p.Phe67Tyr
NM_032446.3:c.200T>A	NP_115822.1:p.Phe67Tyr
NM_001308119.2:c.200T>A	NP_001295048.1:p.Phe67Tyr
NM_001308121.2:c.200T>A	NP_001295050.1:p.Phe67Tyr