Canonical Allele Identifier: CA7677964

Gene: LINGO1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77615442G>A , CM000677.2:g.77615442G>A	GRCh38
NC_000015.9:g.77907784G>A , CM000677.1:g.77907784G>A	GRCh37
NC_000015.8:g.75694839G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355300.7:c.465C>T MANE Select	ENSP00000347451.6:p.Ile155=
ENST00000355300.6:c.465C>T	ENSP00000347451.6:p.Ile155=
ENST00000557798.1:c.480C>T	ENSP00000453780.1:p.Ile160=
ENST00000561030.5:c.447C>T	ENSP00000453853.1:p.Ile149=
ENST00000561686.5:c.447C>T	ENSP00000455605.1:p.Ile149=
NM_001301186.1:c.447C>T	NP_001288115.1:p.Ile149=
NM_001301187.1:c.447C>T	NP_001288116.1:p.Ile149=
NM_001301189.1:c.447C>T	NP_001288118.1:p.Ile149=
NM_001301191.1:c.447C>T	NP_001288120.1:p.Ile149=
NM_001301192.1:c.447C>T	NP_001288121.1:p.Ile149=
NM_001301194.1:c.447C>T	NP_001288123.1:p.Ile149=
NM_001301195.1:c.447C>T	NP_001288124.1:p.Ile149=
NM_001301197.1:c.447C>T	NP_001288126.1:p.Ile149=
NM_001301198.1:c.447C>T	NP_001288127.1:p.Ile149=
NM_001301199.1:c.447C>T	NP_001288128.1:p.Ile149=
NM_001301200.1:c.447C>T	NP_001288129.1:p.Ile149=
NM_032808.6:c.465C>T	NP_116197.4:p.Ile155=
XM_011522117.1:c.447C>T	XP_011520419.1:p.Ile149=
XM_011522118.1:c.447C>T	XP_011520420.1:p.Ile149=
XM_011522118.2:c.447C>T	XP_011520420.1:p.Ile149=
XM_017022682.1:c.447C>T	XP_016878171.1:p.Ile149=
XM_024450091.1:c.447C>T	XP_024305859.1:p.Ile149=
XR_001751806.1:n.690-14843G>A
NM_001301189.2:c.447C>T	NP_001288118.1:p.Ile149=
NM_001301191.2:c.447C>T	NP_001288120.1:p.Ile149=
NM_001301192.2:c.447C>T	NP_001288121.1:p.Ile149=
NM_001301194.2:c.447C>T	NP_001288123.1:p.Ile149=
NM_001301195.2:c.447C>T	NP_001288124.1:p.Ile149=
NM_001301200.2:c.447C>T	NP_001288129.1:p.Ile149=
NM_032808.7:c.465C>T MANE Select	NP_116197.4:p.Ile155=
NM_001301186.2:c.447C>T	NP_001288115.1:p.Ile149=
NM_001301187.2:c.447C>T	NP_001288116.1:p.Ile149=
NM_001301197.2:c.447C>T	NP_001288126.1:p.Ile149=
NM_001301198.2:c.447C>T	NP_001288127.1:p.Ile149=
NM_001301199.2:c.447C>T	NP_001288128.1:p.Ile149=