Canonical Allele Identifier: CA7759526

Gene: LINS1

Linked Data

• dbSNP Id: rs779666703
• ExAC: 15:101113942 T / C
• gnomAD v2: 15-101113942-T-C
• gnomAD v3: 15-100573737-T-C
• gnomAD v4: 15-100573737-T-C
• MyVariant Identifiers: chr15:g.101113942T>C (hg19) ; chr15:g.100573737T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100573737T>C , CM000677.2:g.100573737T>C	GRCh38
NC_000015.9:g.101113942T>C , CM000677.1:g.101113942T>C	GRCh37
NC_000015.8:g.98931465T>C	NCBI36
NG_034076.1:g.33504A>G
NG_034076.2:g.34296A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314742.13:c.1136A>G MANE Select	ENSP00000318423.8:p.His379Arg
ENST00000314742.12:c.1136A>G	ENSP00000318423.8:p.His379Arg
ENST00000559149.5:n.1293A>G
ENST00000560133.5:c.779A>G	ENSP00000454929.1:p.His260Arg
ENST00000560783.1:c.105A>G
ENST00000561308.5:c.1136A>G	ENSP00000454200.1:p.His379Arg
NM_001040616.2:c.1136A>G	NP_001035706.1:p.His379Arg
XM_005254941.1:c.1136A>G	XP_005254998.1:p.His379Arg
XM_005254943.1:c.1136A>G	XP_005255000.1:p.His379Arg
XR_243210.2:n.1239A>G
XR_429464.2:n.1239A>G
XR_931862.1:n.1239A>G
XR_931863.1:n.1239A>G
XR_931864.1:n.1239A>G
NM_001352507.1:c.389A>G	NP_001339436.1:p.His130Arg
NM_001352508.1:c.1091A>G	NP_001339437.1:p.His364Arg
NR_148017.1:n.1359A>G
NR_148018.1:n.1359A>G
NR_148019.1:n.1363A>G
XM_005254941.2:c.1136A>G	XP_005254998.1:p.His379Arg
XM_005254943.2:c.1136A>G	XP_005255000.1:p.His379Arg
XM_017022399.2:c.389A>G	XP_016877888.1:p.His130Arg
XM_017022400.2:c.389A>G	XP_016877889.1:p.His130Arg
XM_024449979.1:c.1136A>G	XP_024305747.1:p.His379Arg
XM_024449980.1:c.1136A>G	XP_024305748.1:p.His379Arg
XR_001751346.2:n.2151A>G
XR_001751347.2:n.2151A>G
XR_001751348.2:n.2151A>G
XR_002957655.1:n.2151A>G
XR_931862.3:n.2151A>G
NM_001040616.3:c.1136A>G MANE Select	NP_001035706.2:p.His379Arg
NM_001352507.2:c.389A>G	NP_001339436.1:p.His130Arg
NM_001352508.2:c.1091A>G	NP_001339437.1:p.His364Arg
NR_148017.2:n.1303A>G
NR_148018.2:n.1303A>G
NR_148019.2:n.1307A>G