Canonical Allele Identifier: CA971730402

Gene: LINGO1

Linked Data

• dbSNP Id: rs2075395056
• gnomAD v3: 15-77680403-CCTTG-C
• gnomAD v4: 15-77680403-CCTTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77680406_77680409del , CM000677.2:g.77680406_77680409del	GRCh38
NC_000015.9:g.77972748_77972751del , CM000677.1:g.77972748_77972751del	GRCh37
NC_000015.8:g.75759803_75759806del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000559893.5:c.-98-3233_-98-3230del	ENSP00000454051.1:n.-98-3233_-98-3230del
ENST00000561030.5:c.-98-3233_-98-3230del	ENSP00000453853.1:n.-98-3233_-98-3230del
ENST00000561686.5:c.-13+10313_-13+10316del	ENSP00000455605.1:n.-13+10313_-13+10316del
ENST00000562933.5:c.-98-3233_-98-3230del	ENSP00000456516.1:n.-98-3233_-98-3230del
ENST00000563316.5:c.-98-3233_-98-3230del	ENSP00000457101.1:n.-98-3233_-98-3230del
ENST00000564066.1:n.551-3233_551-3230del
ENST00000564472.5:c.-98-3233_-98-3230del	ENSP00000454245.1:n.-98-3233_-98-3230del
ENST00000566711.5:c.-98-3233_-98-3230del	ENSP00000454687.1:n.-98-3233_-98-3230del
ENST00000567605.5:n.618-3233_618-3230del
ENST00000567726.5:c.-98-3233_-98-3230del	ENSP00000454465.1:n.-98-3233_-98-3230del
ENST00000568951.5:n.436-3233_436-3230del
ENST00000570216.5:c.-98-3233_-98-3230del	ENSP00000454577.1:n.-98-3233_-98-3230del
NM_001301186.1:c.-98-3233_-98-3230del	NP_001288115.1:n.-98-3233_-98-3230del
NM_001301187.1:c.-98-3233_-98-3230del	NP_001288116.1:n.-98-3233_-98-3230del
NM_001301189.1:c.-98-3233_-98-3230del	NP_001288118.1:n.-98-3233_-98-3230del
NM_001301191.1:c.-98-3233_-98-3230del	NP_001288120.1:n.-98-3233_-98-3230del
NM_001301192.1:c.-98-3233_-98-3230del	NP_001288121.1:n.-98-3233_-98-3230del
NM_001301194.1:c.-98-3233_-98-3230del	NP_001288123.1:n.-98-3233_-98-3230del
NM_001301195.1:c.-13+10313_-13+10316del	NP_001288124.1:n.-13+10313_-13+10316del
NM_001301197.1:c.-98-3233_-98-3230del	NP_001288126.1:n.-98-3233_-98-3230del
NM_001301198.1:c.-98-3233_-98-3230del	NP_001288127.1:n.-98-3233_-98-3230del
NM_001301199.1:c.-98-3233_-98-3230del	NP_001288128.1:n.-98-3233_-98-3230del
NM_001301200.1:c.-98-3233_-98-3230del	NP_001288129.1:n.-98-3233_-98-3230del
XM_011522117.1:c.-98-3233_-98-3230del	XP_011520419.1:n.-98-3233_-98-3230del
XM_017022682.1:c.-98-3233_-98-3230del	XP_016878171.1:n.-98-3233_-98-3230del
XM_024450091.1:c.-98-3233_-98-3230del	XP_024305859.1:n.-98-3233_-98-3230del
NM_001301189.2:c.-98-3233_-98-3230del	NP_001288118.1:n.-98-3233_-98-3230del
NM_001301191.2:c.-98-3233_-98-3230del	NP_001288120.1:n.-98-3233_-98-3230del
NM_001301192.2:c.-98-3233_-98-3230del	NP_001288121.1:n.-98-3233_-98-3230del
NM_001301194.2:c.-98-3233_-98-3230del	NP_001288123.1:n.-98-3233_-98-3230del
NM_001301195.2:c.-13+10313_-13+10316del	NP_001288124.1:n.-13+10313_-13+10316del
NM_001301200.2:c.-98-3233_-98-3230del	NP_001288129.1:n.-98-3233_-98-3230del
NM_001301186.2:c.-98-3233_-98-3230del	NP_001288115.1:n.-98-3233_-98-3230del
NM_001301187.2:c.-98-3233_-98-3230del	NP_001288116.1:n.-98-3233_-98-3230del
NM_001301197.2:c.-98-3233_-98-3230del	NP_001288126.1:n.-98-3233_-98-3230del
NM_001301198.2:c.-98-3233_-98-3230del	NP_001288127.1:n.-98-3233_-98-3230del
NM_001301199.2:c.-98-3233_-98-3230del	NP_001288128.1:n.-98-3233_-98-3230del