Canonical Allele Identifier: CA562701213

Gene: MEGF10

Linked Data

• dbSNP Id: rs1353926922
• gnomAD v2: 5-126778492-C-T
• gnomAD v3: 5-127442800-C-T
• gnomAD v4: 5-127442800-C-T
• MyVariant Identifiers: chr5:g.126778492C>T (hg19) ; chr5:g.127442800C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127442800C>T , CM000667.2:g.127442800C>T	GRCh38
NC_000005.9:g.126778492C>T , CM000667.1:g.126778492C>T	GRCh37
NC_000005.8:g.126806391C>T	NCBI36
NG_032072.1:g.157037C>T
NG_032072.2:g.157037C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503335.7:c.2363-198C>T MANE Select	ENSP00000423354.2:n.2363-198C>T
ENST00000274473.6:c.2363-198C>T	ENSP00000274473.6:n.2363-198C>T
ENST00000503335.6:c.2363-198C>T	ENSP00000423354.2:n.2363-198C>T
NM_001256545.1:c.2363-198C>T	NP_001243474.1:n.2363-198C>T
NM_032446.2:c.2363-198C>T	NP_115822.1:n.2363-198C>T
XM_011543692.1:c.2363-198C>T	XP_011541994.1:n.2363-198C>T
XM_011543693.1:c.2363-198C>T	XP_011541995.1:n.2363-198C>T
XM_011543694.1:c.2363-198C>T	XP_011541996.1:n.2363-198C>T
XM_017009987.1:c.2528-198C>T	XP_016865476.1:n.2528-198C>T
XM_017009988.1:c.1223-198C>T	XP_016865477.1:n.1223-198C>T
NM_001256545.2:c.2363-198C>T MANE Select	NP_001243474.1:n.2363-198C>T
NM_032446.3:c.2363-198C>T	NP_115822.1:n.2363-198C>T