Canonical Allele Identifier: CA2675090183

Gene: MEGF10

Linked Data

• gnomAD v4: 5-127442945-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127442945C>T , CM000667.2:g.127442945C>T	GRCh38
NC_000005.9:g.126778637C>T , CM000667.1:g.126778637C>T	GRCh37
NC_000005.8:g.126806536C>T	NCBI36
NG_032072.1:g.157182C>T
NG_032072.2:g.157182C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000503335.7:c.2363-53C>T MANE Select	ENSP00000423354.2:n.2363-53C>T
ENST00000274473.6:c.2363-53C>T	ENSP00000274473.6:n.2363-53C>T
ENST00000503335.6:c.2363-53C>T	ENSP00000423354.2:n.2363-53C>T
NM_001256545.1:c.2363-53C>T	NP_001243474.1:n.2363-53C>T
NM_032446.2:c.2363-53C>T	NP_115822.1:n.2363-53C>T
XM_011543692.1:c.2363-53C>T	XP_011541994.1:n.2363-53C>T
XM_011543693.1:c.2363-53C>T	XP_011541995.1:n.2363-53C>T
XM_011543694.1:c.2363-53C>T	XP_011541996.1:n.2363-53C>T
XM_017009987.1:c.2528-53C>T	XP_016865476.1:n.2528-53C>T
XM_017009988.1:c.1223-53C>T	XP_016865477.1:n.1223-53C>T
NM_001256545.2:c.2363-53C>T MANE Select	NP_001243474.1:n.2363-53C>T
NM_032446.3:c.2363-53C>T	NP_115822.1:n.2363-53C>T