Canonical Allele Identifier: CA715894454

Gene: LINGO1

Linked Data

• dbSNP Id: rs1396692121
• MyVariant Identifiers: chr15:g.77963835_77963837del (hg19) ; chr15:g.77671493_77671495del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77671497_77671499del , CM000677.2:g.77671497_77671499del	GRCh38
NC_000015.9:g.77963839_77963841del , CM000677.1:g.77963839_77963841del	GRCh37
NC_000015.8:g.75750894_75750896del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000559893.5:c.-13+5594_-13+5596del	ENSP00000454051.1:n.-13+5594_-13+5596del
ENST00000561030.5:c.-13+5594_-13+5596del	ENSP00000453853.1:n.-13+5594_-13+5596del
ENST00000561686.5:c.-13+19225_-13+19227del	ENSP00000455605.1:n.-13+19225_-13+19227del
ENST00000562933.5:c.-13+5594_-13+5596del	ENSP00000456516.1:n.-13+5594_-13+5596del
ENST00000563316.5:c.-13+5594_-13+5596del	ENSP00000457101.1:n.-13+5594_-13+5596del
ENST00000564472.5:c.-13+5594_-13+5596del	ENSP00000454245.1:n.-13+5594_-13+5596del
ENST00000566711.5:c.-13+5594_-13+5596del	ENSP00000454687.1:n.-13+5594_-13+5596del
ENST00000567726.5:c.-13+5594_-13+5596del	ENSP00000454465.1:n.-13+5594_-13+5596del
ENST00000570216.5:c.-13+5594_-13+5596del	ENSP00000454577.1:n.-13+5594_-13+5596del
NM_001301186.1:c.-13+5594_-13+5596del	NP_001288115.1:n.-13+5594_-13+5596del
NM_001301187.1:c.-13+5594_-13+5596del	NP_001288116.1:n.-13+5594_-13+5596del
NM_001301189.1:c.-13+5594_-13+5596del	NP_001288118.1:n.-13+5594_-13+5596del
NM_001301191.1:c.-13+5594_-13+5596del	NP_001288120.1:n.-13+5594_-13+5596del
NM_001301192.1:c.-13+5594_-13+5596del	NP_001288121.1:n.-13+5594_-13+5596del
NM_001301194.1:c.-13+5594_-13+5596del	NP_001288123.1:n.-13+5594_-13+5596del
NM_001301195.1:c.-13+19225_-13+19227del	NP_001288124.1:n.-13+19225_-13+19227del
NM_001301197.1:c.-13+5594_-13+5596del	NP_001288126.1:n.-13+5594_-13+5596del
NM_001301198.1:c.-13+5594_-13+5596del	NP_001288127.1:n.-13+5594_-13+5596del
NM_001301199.1:c.-13+5594_-13+5596del	NP_001288128.1:n.-13+5594_-13+5596del
NM_001301200.1:c.-13+5594_-13+5596del	NP_001288129.1:n.-13+5594_-13+5596del
XM_011522117.1:c.-13+5594_-13+5596del	XP_011520419.1:n.-13+5594_-13+5596del
XM_011522118.1:c.-13+187_-13+189del	XP_011520420.1:n.-13+187_-13+189del
XM_011522118.2:c.-13+187_-13+189del	XP_011520420.1:n.-13+187_-13+189del
XM_017022682.1:c.-13+5594_-13+5596del	XP_016878171.1:n.-13+5594_-13+5596del
XM_024450091.1:c.-13+5594_-13+5596del	XP_024305859.1:n.-13+5594_-13+5596del
NM_001301189.2:c.-13+5594_-13+5596del	NP_001288118.1:n.-13+5594_-13+5596del
NM_001301191.2:c.-13+5594_-13+5596del	NP_001288120.1:n.-13+5594_-13+5596del
NM_001301192.2:c.-13+5594_-13+5596del	NP_001288121.1:n.-13+5594_-13+5596del
NM_001301194.2:c.-13+5594_-13+5596del	NP_001288123.1:n.-13+5594_-13+5596del
NM_001301195.2:c.-13+19225_-13+19227del	NP_001288124.1:n.-13+19225_-13+19227del
NM_001301200.2:c.-13+5594_-13+5596del	NP_001288129.1:n.-13+5594_-13+5596del
NM_001301186.2:c.-13+5594_-13+5596del	NP_001288115.1:n.-13+5594_-13+5596del
NM_001301187.2:c.-13+5594_-13+5596del	NP_001288116.1:n.-13+5594_-13+5596del
NM_001301197.2:c.-13+5594_-13+5596del	NP_001288126.1:n.-13+5594_-13+5596del
NM_001301198.2:c.-13+5594_-13+5596del	NP_001288127.1:n.-13+5594_-13+5596del
NM_001301199.2:c.-13+5594_-13+5596del	NP_001288128.1:n.-13+5594_-13+5596del