Canonical Allele Identifier: CA13061438

Gene: LINGO2

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.28181087C>T , CM000671.2:g.28181087C>T	GRCh38
NC_000009.11:g.28181085C>T , CM000671.1:g.28181085C>T	GRCh37
NC_000009.10:g.28171085C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698399.1:c.-36+114121G>A MANE Select	ENSP00000513694.1:n.-36+114121G>A
ENST00000698400.1:c.-250-100109G>A	ENSP00000513695.1:n.-250-100109G>A
ENST00000698401.1:c.-439+114121G>A	ENSP00000513696.1:n.-439+114121G>A
ENST00000698402.1:c.-190-100109G>A	ENSP00000513697.1:n.-190-100109G>A
ENST00000698403.1:c.-411-100109G>A	ENSP00000513698.1:n.-411-100109G>A
ENST00000698404.1:c.-147+114121G>A	ENSP00000513699.1:n.-147+114121G>A
ENST00000308675.5:c.-111-51414G>A	ENSP00000310126.3:n.-111-51414G>A
ENST00000379992.6:c.-87+114121G>A	ENSP00000369328.1:n.-87+114121G>A
ENST00000493941.1:n.125-100109G>A
ENST00000613945.3:c.-60-51414G>A	ENSP00000479634.1:n.-60-51414G>A
NM_001258282.1:c.-36+114121G>A	NP_001245211.1:n.-36+114121G>A
NM_152570.2:c.-87+114121G>A	NP_689783.1:n.-87+114121G>A
XM_011517715.1:c.-36+114121G>A	XP_011516017.1:n.-36+114121G>A
XM_011517716.1:c.-36+114121G>A	XP_011516018.1:n.-36+114121G>A
XM_011517717.1:c.-36+114121G>A	XP_011516019.1:n.-36+114121G>A
XM_011517718.1:c.-36+114121G>A	XP_011516020.1:n.-36+114121G>A
XM_011517719.1:c.-36+114121G>A	XP_011516021.1:n.-36+114121G>A
NM_001258282.2:c.-36+114121G>A	NP_001245211.1:n.-36+114121G>A
NM_001354574.1:c.-36+114121G>A	NP_001341503.1:n.-36+114121G>A
NM_001354575.1:c.-36+114121G>A	NP_001341504.1:n.-36+114121G>A
NM_152570.3:c.-87+114121G>A	NP_689783.1:n.-87+114121G>A
XM_017014303.2:c.-2661+114121G>A	XP_016869792.1:n.-2661+114121G>A
XR_001746186.2:n.2518+114121G>A
NM_001258282.3:c.-36+114121G>A MANE Select	NP_001245211.1:n.-36+114121G>A
NM_001354574.2:c.-36+114121G>A	NP_001341503.1:n.-36+114121G>A
NM_001354575.2:c.-36+114121G>A	NP_001341504.1:n.-36+114121G>A
NM_152570.4:c.-87+114121G>A	NP_689783.1:n.-87+114121G>A