Canonical Allele Identifier: CA2390315517

Gene: MX1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.41426138G= , CM000683.2:g.41426138G=	GRCh38
NC_000021.8:g.42798065G= , CM000683.1:g.42798065G=	GRCh37
NC_000021.7:g.41719935G=	NCBI36
NG_027788.1:g.10546G=
NG_027788.2:g.10546G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001144925.2:c.-308-1068G=	NP_001138397.1:n.-308-1068G=
NM_001178046.2:c.-259G=	NP_001171517.1:n.-259G=
NM_002462.4:c.-434G=	NP_002453.2:n.-434G=
ENST00000398600.6:c.-308-1068G=	ENSP00000381601.2:n.-308-1068G=
ENST00000413778.5:c.-327-1068G=	ENSP00000408498.1:n.-327-1068G=
ENST00000413778.6:c.-327-1068G=	ENSP00000408498.2:n.-327-1068G=
ENST00000419044.5:c.-332G=	ENSP00000392151.1:n.-332G=
ENST00000419044.6:c.-332G=	ENSP00000392151.2:n.-332G=
ENST00000455164.6:c.-259G=	ENSP00000410523.2:n.-259G=
ENST00000486275.2:n.473-1068G=
ENST00000490220.5:n.552-1068G=
ENST00000679445.1:c.-308-1068G=	ENSP00000505630.1:n.-308-1068G=
ENST00000679464.1:c.-209-1617G=	ENSP00000505874.1:n.-209-1617G=
ENST00000679626.1:c.-209-1617G=	ENSP00000506481.1:n.-209-1617G=
ENST00000679705.1:c.-351G=	ENSP00000506372.1:n.-351G=
ENST00000679911.1:c.-308-1068G=	ENSP00000505189.1:n.-308-1068G=
ENST00000680182.1:c.-308-1068G=	ENSP00000506395.1:n.-308-1068G=
ENST00000680347.1:c.-308-1068G=	ENSP00000506183.1:n.-308-1068G=
ENST00000681191.1:c.-308-1068G=	ENSP00000505657.1:n.-308-1068G=
ENST00000681415.1:c.-308-1068G=	ENSP00000506062.1:n.-308-1068G=
ENST00000681849.1:c.-335G=	ENSP00000505051.1:n.-335G=
ENST00000681857.1:c.-209-1617G=	ENSP00000505669.1:n.-209-1617G=
ENST00000681867.1:c.-327-1068G=	ENSP00000506690.1:n.-327-1068G=
XM_005260979.1:c.-332G=	XP_005261036.1:n.-332G=
XM_005260979.2:c.-332G=	XP_005261036.1:n.-332G=
XM_011529568.1:c.-308-1068G=	XP_011527870.1:n.-308-1068G=
XM_011529568.2:c.-308-1068G=	XP_011527870.1:n.-308-1068G=
XM_017028349.2:c.-327-1068G=	XP_016883838.1:n.-327-1068G=
XM_017028350.1:c.-351G=	XP_016883839.1:n.-351G=
XM_017028351.2:c.-434G=	XP_016883840.1:n.-434G=