Canonical Allele Identifier: CA2390291637

Gene: MX2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.41374246T= , CM000683.2:g.41374246T=	GRCh38
NC_000021.8:g.42746173T= , CM000683.1:g.42746173T=	GRCh37
NC_000021.7:g.41668043T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330714.8:c.-71-2590T= MANE Select	ENSP00000333657.3:n.-71-2590T=
ENST00000418103.2:c.-71-2590T=	ENSP00000410188.2:n.-71-2590T=
ENST00000435611.6:c.-71-2590T=	ENSP00000389256.2:n.-71-2590T=
ENST00000680862.1:c.-71-2590T=	ENSP00000506423.1:n.-71-2590T=
ENST00000330714.7:c.-71-2590T=	ENSP00000333657.3:n.-71-2590T=
ENST00000416447.1:c.-72+119T=	ENSP00000411179.1:n.-72+119T=
ENST00000418103.1:c.-71-2590T=	ENSP00000410188.1:n.-71-2590T=
ENST00000435611.5:c.-71-2590T=	ENSP00000389256.1:n.-71-2590T=
ENST00000436410.5:c.-72+1247T=	ENSP00000393975.1:n.-72+1247T=
NM_002463.1:c.-71-2590T=	NP_002454.1:n.-71-2590T=
XM_005260983.3:c.-71-2590T=	XP_005261040.1:n.-71-2590T=
XM_005260984.1:c.-71-2590T=	XP_005261041.1:n.-71-2590T=
XM_011529571.1:c.-72+1247T=	XP_011527873.1:n.-72+1247T=
XM_011529572.1:c.-72+119T=	XP_011527874.1:n.-72+119T=
XM_011529573.1:c.-71-2590T=	XP_011527875.1:n.-71-2590T=
XM_005260983.5:c.-71-2590T=	XP_005261040.1:n.-71-2590T=
XM_011529572.2:c.-72+119T=	XP_011527874.1:n.-72+119T=
XM_011529573.2:c.-71-2590T=	XP_011527875.1:n.-71-2590T=
XM_024452080.1:c.-71-2590T=	XP_024307848.1:n.-71-2590T=
NM_002463.2:c.-71-2590T= MANE Select	NP_002454.1:n.-71-2590T=