Canonical Allele Identifier: CA1842635084

Gene: LINGO2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.28402045A= , CM000671.2:g.28402045A=	GRCh38
NC_000009.11:g.28402043A= , CM000671.1:g.28402043A=	GRCh37
NC_000009.10:g.28392043A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001258282.3:c.-227-29177T= MANE Select	NP_001245211.1:n.-227-29177T=
ENST00000698399.1:c.-227-29177T= MANE Select	ENSP00000513694.1:n.-227-29177T=
NM_001258282.1:c.-227-29177T=	NP_001245211.1:n.-227-29177T=
NM_001258282.2:c.-227-29177T=	NP_001245211.1:n.-227-29177T=
NM_001354574.1:c.-195+73895T=	NP_001341503.1:n.-195+73895T=
NM_001354574.2:c.-195+73895T=	NP_001341503.1:n.-195+73895T=
NM_001354575.1:c.-227-29177T=	NP_001341504.1:n.-227-29177T=
NM_001354575.2:c.-227-29177T=	NP_001341504.1:n.-227-29177T=
NM_152570.2:c.-278-29177T=	NP_689783.1:n.-278-29177T=
NM_152570.3:c.-278-29177T=	NP_689783.1:n.-278-29177T=
NM_152570.4:c.-278-29177T=	NP_689783.1:n.-278-29177T=
ENST00000308675.5:c.-261+73882T=	ENSP00000310126.3:n.-261+73882T=
ENST00000379992.6:c.-278-29177T=	ENSP00000369328.1:n.-278-29177T=
ENST00000613945.3:c.-210+73882T=	ENSP00000479634.1:n.-210+73882T=
ENST00000698400.1:c.-442-29177T=	ENSP00000513695.1:n.-442-29177T=
ENST00000698401.1:c.-598+73895T=	ENSP00000513696.1:n.-598+73895T=
ENST00000698402.1:c.-382-29177T=	ENSP00000513697.1:n.-382-29177T=
ENST00000698403.1:c.-603-29177T=	ENSP00000513698.1:n.-603-29177T=
ENST00000698404.1:c.-338-29177T=	ENSP00000513699.1:n.-338-29177T=
XM_011517715.1:c.-227-29177T=	XP_011516017.1:n.-227-29177T=
XM_011517716.1:c.-227-29177T=	XP_011516018.1:n.-227-29177T=
XM_011517717.1:c.-227-29177T=	XP_011516019.1:n.-227-29177T=
XM_011517718.1:c.-227-29177T=	XP_011516020.1:n.-227-29177T=
XM_011517719.1:c.-195+73895T=	XP_011516021.1:n.-195+73895T=
XM_017014303.2:c.-2852-29177T=	XP_016869792.1:n.-2852-29177T=
XR_001746186.2:n.2327-29177T=