Canonical Allele Identifier: CA14198919
Gene: LINGO1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11856808

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.77680428C>T , CM000677.2:g.77680428C>T GRCh38
NC_000015.8:g.75759825C>T NCBI36
NC_000015.9:g.77972770C>T , CM000677.1:g.77972770C>T GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000559893.5:c.-98-3254G>A ENSP00000454051.1:p.=
ENST00000561030.5:c.-98-3254G>A ENSP00000453853.1:p.=
ENST00000561686.5:c.-13+10292G>A ENSP00000455605.1:p.=
ENST00000562933.5:c.-98-3254G>A ENSP00000456516.1:p.=
ENST00000563316.5:c.-98-3254G>A ENSP00000457101.1:p.=
ENST00000564066.1:n.551-3254G>A
ENST00000564472.5:c.-98-3254G>A ENSP00000454245.1:p.=
ENST00000566711.5:c.-98-3254G>A ENSP00000454687.1:p.=
ENST00000567605.5:n.618-3254G>A
ENST00000567726.5:c.-98-3254G>A ENSP00000454465.1:p.=
ENST00000568951.5:n.436-3254G>A
ENST00000570216.5:c.-98-3254G>A ENSP00000454577.1:p.=
NM_001301186.1:c.-98-3254G>A VV NP_001288115.1:p.=
NM_001301187.1:c.-98-3254G>A VV NP_001288116.1:p.=
NM_001301189.1:c.-98-3254G>A VV NP_001288118.1:p.=
NM_001301191.1:c.-98-3254G>A VV NP_001288120.1:p.=
NM_001301192.1:c.-98-3254G>A VV NP_001288121.1:p.=
NM_001301194.1:c.-98-3254G>A VV NP_001288123.1:p.=
NM_001301195.1:c.-13+10292G>A VV NP_001288124.1:p.=
NM_001301197.1:c.-98-3254G>A VV NP_001288126.1:p.=
NM_001301198.1:c.-98-3254G>A VV NP_001288127.1:p.=
NM_001301199.1:c.-98-3254G>A VV NP_001288128.1:p.=
NM_001301200.1:c.-98-3254G>A VV NP_001288129.1:p.=
XM_011522117.1:c.-98-3254G>A XP_011520419.1:p.=
XM_017022682.1:c.-98-3254G>A XP_016878171.1:p.=
XM_024450091.1:c.-98-3254G>A XP_024305859.1:p.=