Canonical Allele Identifier: CA7677751

Gene: LINGO1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77614350G>A , CM000677.2:g.77614350G>A	GRCh38
NC_000015.9:g.77906692G>A , CM000677.1:g.77906692G>A	GRCh37
NC_000015.8:g.75693747G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355300.7:c.1557C>T MANE Select	ENSP00000347451.6:p.Pro519=
ENST00000355300.6:c.1557C>T	ENSP00000347451.6:p.Pro519=
ENST00000561030.5:c.1539C>T	ENSP00000453853.1:p.Pro513=
NM_001301186.1:c.1539C>T	NP_001288115.1:p.Pro513=
NM_001301187.1:c.1539C>T	NP_001288116.1:p.Pro513=
NM_001301189.1:c.1539C>T	NP_001288118.1:p.Pro513=
NM_001301191.1:c.1539C>T	NP_001288120.1:p.Pro513=
NM_001301192.1:c.1539C>T	NP_001288121.1:p.Pro513=
NM_001301194.1:c.1539C>T	NP_001288123.1:p.Pro513=
NM_001301195.1:c.1539C>T	NP_001288124.1:p.Pro513=
NM_001301197.1:c.1539C>T	NP_001288126.1:p.Pro513=
NM_001301198.1:c.1539C>T	NP_001288127.1:p.Pro513=
NM_001301199.1:c.1539C>T	NP_001288128.1:p.Pro513=
NM_001301200.1:c.1539C>T	NP_001288129.1:p.Pro513=
NM_032808.6:c.1557C>T	NP_116197.4:p.Pro519=
XM_011522117.1:c.1539C>T	XP_011520419.1:p.Pro513=
XM_011522118.1:c.1539C>T	XP_011520420.1:p.Pro513=
XM_011522118.2:c.1539C>T	XP_011520420.1:p.Pro513=
XM_017022682.1:c.1539C>T	XP_016878171.1:p.Pro513=
XM_024450091.1:c.1539C>T	XP_024305859.1:p.Pro513=
XR_001751806.1:n.690-15935G>A
NM_001301189.2:c.1539C>T	NP_001288118.1:p.Pro513=
NM_001301191.2:c.1539C>T	NP_001288120.1:p.Pro513=
NM_001301192.2:c.1539C>T	NP_001288121.1:p.Pro513=
NM_001301194.2:c.1539C>T	NP_001288123.1:p.Pro513=
NM_001301195.2:c.1539C>T	NP_001288124.1:p.Pro513=
NM_001301200.2:c.1539C>T	NP_001288129.1:p.Pro513=
NM_032808.7:c.1557C>T MANE Select	NP_116197.4:p.Pro519=
NM_001301186.2:c.1539C>T	NP_001288115.1:p.Pro513=
NM_001301187.2:c.1539C>T	NP_001288116.1:p.Pro513=
NM_001301197.2:c.1539C>T	NP_001288126.1:p.Pro513=
NM_001301198.2:c.1539C>T	NP_001288127.1:p.Pro513=
NM_001301199.2:c.1539C>T	NP_001288128.1:p.Pro513=