Canonical Allele Identifier: CA2390294669

Gene: MX2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.41380446T= , CM000683.2:g.41380446T=	GRCh38
NC_000021.8:g.42752373T= , CM000683.1:g.42752373T=	GRCh37
NC_000021.7:g.41674243T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330714.8:c.577+295T= MANE Select	ENSP00000333657.3:n.577+295T=
ENST00000418103.2:c.443-1964T=	ENSP00000410188.2:n.443-1964T=
ENST00000435611.6:c.577+295T=	ENSP00000389256.2:n.577+295T=
ENST00000493753.2:n.634+295T=
ENST00000680862.1:c.577+295T=	ENSP00000506423.1:n.577+295T=
ENST00000330714.7:c.577+295T=	ENSP00000333657.3:n.577+295T=
NM_002463.1:c.577+295T=	NP_002454.1:n.577+295T=
XM_005260983.3:c.577+295T=	XP_005261040.1:n.577+295T=
XM_005260984.1:c.577+295T=	XP_005261041.1:n.577+295T=
XM_011529571.1:c.577+295T=	XP_011527873.1:n.577+295T=
XM_011529572.1:c.577+295T=	XP_011527874.1:n.577+295T=
XM_011529573.1:c.443-1964T=	XP_011527875.1:n.443-1964T=
XM_005260983.5:c.577+295T=	XP_005261040.1:n.577+295T=
XM_011529572.2:c.577+295T=	XP_011527874.1:n.577+295T=
XM_011529573.2:c.443-1964T=	XP_011527875.1:n.443-1964T=
XM_024452080.1:c.577+295T=	XP_024307848.1:n.577+295T=
NM_002463.2:c.577+295T= MANE Select	NP_002454.1:n.577+295T=