Canonical Allele Identifier: CA492684235

Gene: LINS1

Linked Data

• MyVariant Identifiers: chr15:g.101113935G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100573730G>A , CM000677.2:g.100573730G>A	GRCh38
NC_000015.9:g.101113935G>A , CM000677.1:g.101113935G>A	GRCh37
NC_000015.8:g.98931458G>A	NCBI36
NG_034076.1:g.33511C>T
NG_034076.2:g.34303C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314742.13:c.1143C>T MANE Select	ENSP00000318423.8:p.Ile381=
ENST00000314742.12:c.1143C>T	ENSP00000318423.8:p.Ile381=
ENST00000559149.5:n.1300C>T
ENST00000560133.5:c.786C>T	ENSP00000454929.1:p.Ile262=
ENST00000560783.1:c.112C>T
ENST00000561308.5:c.1143C>T	ENSP00000454200.1:p.Ile381=
NM_001040616.2:c.1143C>T	NP_001035706.1:p.Ile381=
XM_005254941.1:c.1143C>T	XP_005254998.1:p.Ile381=
XM_005254943.1:c.1143C>T	XP_005255000.1:p.Ile381=
XR_243210.2:n.1246C>T
XR_429464.2:n.1246C>T
XR_931862.1:n.1246C>T
XR_931863.1:n.1246C>T
XR_931864.1:n.1246C>T
NM_001352507.1:c.396C>T	NP_001339436.1:p.Ile132=
NM_001352508.1:c.1098C>T	NP_001339437.1:p.Ile366=
NR_148017.1:n.1366C>T
NR_148018.1:n.1366C>T
NR_148019.1:n.1370C>T
XM_005254941.2:c.1143C>T	XP_005254998.1:p.Ile381=
XM_005254943.2:c.1143C>T	XP_005255000.1:p.Ile381=
XM_017022399.2:c.396C>T	XP_016877888.1:p.Ile132=
XM_017022400.2:c.396C>T	XP_016877889.1:p.Ile132=
XM_024449979.1:c.1143C>T	XP_024305747.1:p.Ile381=
XM_024449980.1:c.1143C>T	XP_024305748.1:p.Ile381=
XR_001751346.2:n.2158C>T
XR_001751347.2:n.2158C>T
XR_001751348.2:n.2158C>T
XR_002957655.1:n.2158C>T
XR_931862.3:n.2158C>T
NM_001040616.3:c.1143C>T MANE Select	NP_001035706.2:p.Ile381=
NM_001352507.2:c.396C>T	NP_001339436.1:p.Ile132=
NM_001352508.2:c.1098C>T	NP_001339437.1:p.Ile366=
NR_148017.2:n.1310C>T
NR_148018.2:n.1310C>T
NR_148019.2:n.1314C>T