Canonical Allele Identifier: CA10622425

Gene: MEGF10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.127458564C>T , CM000667.2:g.127458564C>T	GRCh38
NC_000005.9:g.126794256C>T , CM000667.1:g.126794256C>T	GRCh37
NC_000005.8:g.126822155C>T	NCBI36
NG_032072.1:g.172801C>T
NG_032072.2:g.172801C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503335.7:c.*1246C>T MANE Select	ENSP00000423354.2:n.*1246C>T
ENST00000274473.6:c.*1246C>T	ENSP00000274473.6:n.*1246C>T
ENST00000503335.6:c.*1246C>T	ENSP00000423354.2:n.*1246C>T
ENST00000515622.1:n.433+2957C>T
NM_001256545.1:c.*1246C>T	NP_001243474.1:n.*1246C>T
NM_032446.2:c.*1246C>T	NP_115822.1:n.*1246C>T
XM_011543692.1:c.*1246C>T	XP_011541994.1:n.*1246C>T
XM_011543693.1:c.*1246C>T	XP_011541995.1:n.*1246C>T
XM_011543694.1:c.*1246C>T	XP_011541996.1:n.*1246C>T
XM_017009987.1:c.*1246C>T	XP_016865476.1:n.*1246C>T
XM_017009988.1:c.*1246C>T	XP_016865477.1:n.*1246C>T
NM_001256545.2:c.*1246C>T MANE Select	NP_001243474.1:n.*1246C>T
NM_032446.3:c.*1246C>T	NP_115822.1:n.*1246C>T