Canonical Allele Identifier: CA562701220

Gene: MEGF10

Linked Data

• dbSNP Id: rs1332368217
• gnomAD v2: 5-126778644-C-A
• gnomAD v4: 5-127442952-C-A
• MyVariant Identifiers: chr5:g.126778644C>A (hg19) ; chr5:g.127442952C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127442952C>A , CM000667.2:g.127442952C>A	GRCh38
NC_000005.9:g.126778644C>A , CM000667.1:g.126778644C>A	GRCh37
NC_000005.8:g.126806543C>A	NCBI36
NG_032072.1:g.157189C>A
NG_032072.2:g.157189C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000503335.7:c.2363-46C>A MANE Select	ENSP00000423354.2:n.2363-46C>A
ENST00000274473.6:c.2363-46C>A	ENSP00000274473.6:n.2363-46C>A
ENST00000503335.6:c.2363-46C>A	ENSP00000423354.2:n.2363-46C>A
NM_001256545.1:c.2363-46C>A	NP_001243474.1:n.2363-46C>A
NM_032446.2:c.2363-46C>A	NP_115822.1:n.2363-46C>A
XM_011543692.1:c.2363-46C>A	XP_011541994.1:n.2363-46C>A
XM_011543693.1:c.2363-46C>A	XP_011541995.1:n.2363-46C>A
XM_011543694.1:c.2363-46C>A	XP_011541996.1:n.2363-46C>A
XM_017009987.1:c.2528-46C>A	XP_016865476.1:n.2528-46C>A
XM_017009988.1:c.1223-46C>A	XP_016865477.1:n.1223-46C>A
NM_001256545.2:c.2363-46C>A MANE Select	NP_001243474.1:n.2363-46C>A
NM_032446.3:c.2363-46C>A	NP_115822.1:n.2363-46C>A