Canonical Allele Identifier: CA1580859277

Gene: MEGF10

Linked Data

• dbSNP Id: rs1580876454

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127442732T>C , CM000667.2:g.127442732T>C	GRCh38
NC_000005.9:g.126778424T>C , CM000667.1:g.126778424T>C	GRCh37
NC_000005.8:g.126806323T>C	NCBI36
NG_032072.1:g.156969T>C
NG_032072.2:g.156969T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503335.7:c.2363-266T>C MANE Select	ENSP00000423354.2:n.2363-266T>C
ENST00000274473.6:c.2363-266T>C	ENSP00000274473.6:n.2363-266T>C
ENST00000503335.6:c.2363-266T>C	ENSP00000423354.2:n.2363-266T>C
NM_001256545.1:c.2363-266T>C	NP_001243474.1:n.2363-266T>C
NM_032446.2:c.2363-266T>C	NP_115822.1:n.2363-266T>C
XM_011543692.1:c.2363-266T>C	XP_011541994.1:n.2363-266T>C
XM_011543693.1:c.2363-266T>C	XP_011541995.1:n.2363-266T>C
XM_011543694.1:c.2363-266T>C	XP_011541996.1:n.2363-266T>C
XM_017009987.1:c.2528-266T>C	XP_016865476.1:n.2528-266T>C
XM_017009988.1:c.1223-266T>C	XP_016865477.1:n.1223-266T>C
NM_001256545.2:c.2363-266T>C MANE Select	NP_001243474.1:n.2363-266T>C
NM_032446.3:c.2363-266T>C	NP_115822.1:n.2363-266T>C