Canonical Allele Identifier: CA14135990
Gene: LINGO1 HGNC NCBI
LINGO1-AS2 HGNC NCBI

Linked Data

dbSNP Id: rs8030859

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.77663174C>T , CM000677.2:g.77663174C>T GRCh38
NC_000015.9:g.77955516C>T , CM000677.1:g.77955516C>T GRCh37
NC_000015.8:g.75742571C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000559893.5:c.-13+13915G>A (LINGO1) ENSP00000454051.1:n.-13+13915G>A
ENST00000561030.5:c.-13+13915G>A (LINGO1) ENSP00000453853.1:n.-13+13915G>A
ENST00000561686.5:c.-13+27546G>A (LINGO1) ENSP00000455605.1:n.-13+27546G>A
ENST00000562933.5:c.-13+13915G>A (LINGO1) ENSP00000456516.1:n.-13+13915G>A
ENST00000563316.5:c.-13+13915G>A (LINGO1) ENSP00000457101.1:n.-13+13915G>A
ENST00000564472.5:c.-13+13915G>A (LINGO1) ENSP00000454245.1:n.-13+13915G>A
ENST00000566711.5:c.-13+13915G>A (LINGO1) ENSP00000454687.1:n.-13+13915G>A
ENST00000567726.5:c.-13+13915G>A (LINGO1) ENSP00000454465.1:n.-13+13915G>A
ENST00000570216.5:c.-13+13915G>A (LINGO1) ENSP00000454577.1:n.-13+13915G>A
NM_001301186.1:c.-13+13915G>A (LINGO1) NP_001288115.1:n.-13+13915G>A
NM_001301187.1:c.-13+13915G>A (LINGO1) NP_001288116.1:n.-13+13915G>A
NM_001301189.1:c.-13+13915G>A (LINGO1) NP_001288118.1:n.-13+13915G>A
NM_001301191.1:c.-13+13915G>A (LINGO1) NP_001288120.1:n.-13+13915G>A
NM_001301192.1:c.-13+13915G>A (LINGO1) NP_001288121.1:n.-13+13915G>A
NM_001301194.1:c.-13+13915G>A (LINGO1) NP_001288123.1:n.-13+13915G>A
NM_001301195.1:c.-13+27546G>A (LINGO1) NP_001288124.1:n.-13+27546G>A
NM_001301197.1:c.-13+13915G>A (LINGO1) NP_001288126.1:n.-13+13915G>A
NM_001301198.1:c.-13+13915G>A (LINGO1) NP_001288127.1:n.-13+13915G>A
NM_001301199.1:c.-13+13915G>A (LINGO1) NP_001288128.1:n.-13+13915G>A
NM_001301200.1:c.-13+13915G>A (LINGO1) NP_001288129.1:n.-13+13915G>A
NR_120361.1:n.133+2991C>T (LINGO1-AS2)
NR_120362.1:n.115+3009C>T (LINGO1-AS2)
XM_011522117.1:c.-13+13915G>A (LINGO1) XP_011520419.1:n.-13+13915G>A
XM_011522118.1:c.-13+8508G>A (LINGO1) XP_011520420.1:n.-13+8508G>A
XM_011522118.2:c.-13+8508G>A (LINGO1) XP_011520420.1:n.-13+8508G>A
XM_017022682.1:c.-13+13915G>A (LINGO1) XP_016878171.1:n.-13+13915G>A
XM_024450091.1:c.-13+13915G>A (LINGO1) XP_024305859.1:n.-13+13915G>A
NM_001301189.2:c.-13+13915G>A (LINGO1) NP_001288118.1:n.-13+13915G>A
NM_001301191.2:c.-13+13915G>A (LINGO1) NP_001288120.1:n.-13+13915G>A
NM_001301192.2:c.-13+13915G>A (LINGO1) NP_001288121.1:n.-13+13915G>A
NM_001301194.2:c.-13+13915G>A (LINGO1) NP_001288123.1:n.-13+13915G>A
NM_001301195.2:c.-13+27546G>A (LINGO1) NP_001288124.1:n.-13+27546G>A
NM_001301200.2:c.-13+13915G>A (LINGO1) NP_001288129.1:n.-13+13915G>A
NM_001301186.2:c.-13+13915G>A (LINGO1) NP_001288115.1:n.-13+13915G>A
NM_001301187.2:c.-13+13915G>A (LINGO1) NP_001288116.1:n.-13+13915G>A
NM_001301197.2:c.-13+13915G>A (LINGO1) NP_001288126.1:n.-13+13915G>A
NM_001301198.2:c.-13+13915G>A (LINGO1) NP_001288127.1:n.-13+13915G>A
NM_001301199.2:c.-13+13915G>A (LINGO1) NP_001288128.1:n.-13+13915G>A