Canonical Allele Identifier: CA14873276
Gene: MX1 HGNC NCBI
gnomAD v4:

Genomic Alleles

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

Transcript Alleles

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