Canonical Allele Identifier: CA2390315504

Gene: MX1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.41426103C= , CM000683.2:g.41426103C=	GRCh38
NC_000021.8:g.42798030C= , CM000683.1:g.42798030C=	GRCh37
NC_000021.7:g.41719900C=	NCBI36
NG_027788.1:g.10511C=
NG_027788.2:g.10511C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001144925.2:c.-308-1103C=	NP_001138397.1:n.-308-1103C=
NM_001178046.2:c.-294C=	NP_001171517.1:n.-294C=
NM_002462.4:c.-469C=	NP_002453.2:n.-469C=
ENST00000398600.6:c.-308-1103C=	ENSP00000381601.2:n.-308-1103C=
ENST00000413778.5:c.-327-1103C=	ENSP00000408498.1:n.-327-1103C=
ENST00000413778.6:c.-327-1103C=	ENSP00000408498.2:n.-327-1103C=
ENST00000419044.5:c.-367C=	ENSP00000392151.1:n.-367C=
ENST00000419044.6:c.-367C=	ENSP00000392151.2:n.-367C=
ENST00000455164.6:c.-294C=	ENSP00000410523.2:n.-294C=
ENST00000486275.2:n.473-1103C=
ENST00000490220.5:n.552-1103C=
ENST00000679445.1:c.-308-1103C=	ENSP00000505630.1:n.-308-1103C=
ENST00000679464.1:c.-209-1652C=	ENSP00000505874.1:n.-209-1652C=
ENST00000679626.1:c.-209-1652C=	ENSP00000506481.1:n.-209-1652C=
ENST00000679705.1:c.-386C=	ENSP00000506372.1:n.-386C=
ENST00000679911.1:c.-308-1103C=	ENSP00000505189.1:n.-308-1103C=
ENST00000680182.1:c.-308-1103C=	ENSP00000506395.1:n.-308-1103C=
ENST00000680347.1:c.-308-1103C=	ENSP00000506183.1:n.-308-1103C=
ENST00000681191.1:c.-308-1103C=	ENSP00000505657.1:n.-308-1103C=
ENST00000681415.1:c.-308-1103C=	ENSP00000506062.1:n.-308-1103C=
ENST00000681849.1:c.-370C=	ENSP00000505051.1:n.-370C=
ENST00000681857.1:c.-209-1652C=	ENSP00000505669.1:n.-209-1652C=
ENST00000681867.1:c.-327-1103C=	ENSP00000506690.1:n.-327-1103C=
XM_005260979.1:c.-367C=	XP_005261036.1:n.-367C=
XM_005260979.2:c.-367C=	XP_005261036.1:n.-367C=
XM_011529568.1:c.-308-1103C=	XP_011527870.1:n.-308-1103C=
XM_011529568.2:c.-308-1103C=	XP_011527870.1:n.-308-1103C=
XM_017028349.2:c.-327-1103C=	XP_016883838.1:n.-327-1103C=
XM_017028350.1:c.-386C=	XP_016883839.1:n.-386C=