Canonical Allele Identifier: CA2830556946
Gene: LINS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.100573764_100573766del , CM000677.2:g.100573764_100573766del GRCh38
NC_000015.9:g.101113969_101113971del , CM000677.1:g.101113969_101113971del GRCh37
NC_000015.8:g.98931492_98931494del NCBI36
NG_034076.1:g.33475_33477del
NG_034076.2:g.34267_34269del

Transcript Alleles

HGVS Amino-acid Change
ENST00000314742.13:c.1107_1109del MANE Select ENSP00000318423.8:p.Glu370del
ENST00000314742.12:c.1107_1109del ENSP00000318423.8:p.Glu370del
ENST00000559149.5:n.1264_1266del
ENST00000560133.5:c.750_752del ENSP00000454929.1:p.Glu251del
ENST00000560783.1:c.76_78del
ENST00000561308.5:c.1107_1109del ENSP00000454200.1:p.Glu370del
NM_001040616.2:c.1107_1109del NP_001035706.1:p.Glu370del
XM_005254941.1:c.1107_1109del XP_005254998.1:p.Glu370del
XM_005254943.1:c.1107_1109del XP_005255000.1:p.Glu370del
XR_243210.2:n.1210_1212del
XR_429464.2:n.1210_1212del
XR_931862.1:n.1210_1212del
XR_931863.1:n.1210_1212del
XR_931864.1:n.1210_1212del
NM_001352507.1:c.360_362del NP_001339436.1:p.Glu121del
NM_001352508.1:c.1062_1064del NP_001339437.1:p.Glu355del
NR_148017.1:n.1330_1332del
NR_148018.1:n.1330_1332del
NR_148019.1:n.1334_1336del
XM_005254941.2:c.1107_1109del XP_005254998.1:p.Glu370del
XM_005254943.2:c.1107_1109del XP_005255000.1:p.Glu370del
XM_017022399.2:c.360_362del XP_016877888.1:p.Glu121del
XM_017022400.2:c.360_362del XP_016877889.1:p.Glu121del
XM_024449979.1:c.1107_1109del XP_024305747.1:p.Glu370del
XM_024449980.1:c.1107_1109del XP_024305748.1:p.Glu370del
XR_001751346.2:n.2122_2124del
XR_001751347.2:n.2122_2124del
XR_001751348.2:n.2122_2124del
XR_002957655.1:n.2122_2124del
XR_931862.3:n.2122_2124del
NM_001040616.3:c.1107_1109del MANE Select NP_001035706.2:p.Glu370del
NM_001352507.2:c.360_362del NP_001339436.1:p.Glu121del
NM_001352508.2:c.1062_1064del NP_001339437.1:p.Glu355del
NR_148017.2:n.1274_1276del
NR_148018.2:n.1274_1276del
NR_148019.2:n.1278_1280del