Canonical Allele Identifier: CA2200116522
Gene: LINS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.100573687T= , CM000677.2:g.100573687T= GRCh38
NC_000015.9:g.101113892T= , CM000677.1:g.101113892T= GRCh37
NC_000015.8:g.98931415T= NCBI36
NG_034076.1:g.33554A=
NG_034076.2:g.34346A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000314742.13:c.1186A= MANE Select ENSP00000318423.8:p.Lys396=
ENST00000314742.12:c.1186A= ENSP00000318423.8:p.Lys396=
ENST00000559149.5:n.1343A=
ENST00000560133.5:c.829A= ENSP00000454929.1:p.Lys277=
ENST00000560783.1:c.155A=
ENST00000561308.5:c.1186A= ENSP00000454200.1:p.Lys396=
NM_001040616.2:c.1186A= NP_001035706.1:p.Lys396=
XM_005254941.1:c.1186A= XP_005254998.1:p.Lys396=
XM_005254943.1:c.1186A= XP_005255000.1:p.Lys396=
XR_243210.2:n.1289A=
XR_429464.2:n.1289A=
XR_931862.1:n.1289A=
XR_931863.1:n.1289A=
XR_931864.1:n.1289A=
NM_001352507.1:c.439A= NP_001339436.1:p.Lys147=
NM_001352508.1:c.1141A= NP_001339437.1:p.Lys381=
NR_148017.1:n.1409A=
NR_148018.1:n.1409A=
NR_148019.1:n.1413A=
XM_005254941.2:c.1186A= XP_005254998.1:p.Lys396=
XM_005254943.2:c.1186A= XP_005255000.1:p.Lys396=
XM_017022399.2:c.439A= XP_016877888.1:p.Lys147=
XM_017022400.2:c.439A= XP_016877889.1:p.Lys147=
XM_024449979.1:c.1186A= XP_024305747.1:p.Lys396=
XM_024449980.1:c.1186A= XP_024305748.1:p.Lys396=
XR_001751346.2:n.2201A=
XR_001751347.2:n.2201A=
XR_001751348.2:n.2201A=
XR_002957655.1:n.2201A=
XR_931862.3:n.2201A=
NM_001040616.3:c.1186A= MANE Select NP_001035706.2:p.Lys396=
NM_001352507.2:c.439A= NP_001339436.1:p.Lys147=
NM_001352508.2:c.1141A= NP_001339437.1:p.Lys381=
NR_148017.2:n.1353A=
NR_148018.2:n.1353A=
NR_148019.2:n.1357A=