Canonical Allele Identifier: CA492684244

Gene: LINS1

Linked Data

• MyVariant Identifiers: chr15:g.101113953A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100573748A>T , CM000677.2:g.100573748A>T	GRCh38
NC_000015.9:g.101113953A>T , CM000677.1:g.101113953A>T	GRCh37
NC_000015.8:g.98931476A>T	NCBI36
NG_034076.1:g.33493T>A
NG_034076.2:g.34285T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314742.13:c.1125T>A MANE Select	ENSP00000318423.8:p.Thr375=
ENST00000314742.12:c.1125T>A	ENSP00000318423.8:p.Thr375=
ENST00000559149.5:n.1282T>A
ENST00000560133.5:c.768T>A	ENSP00000454929.1:p.Thr256=
ENST00000560783.1:c.94T>A
ENST00000561308.5:c.1125T>A	ENSP00000454200.1:p.Thr375=
NM_001040616.2:c.1125T>A	NP_001035706.1:p.Thr375=
XM_005254941.1:c.1125T>A	XP_005254998.1:p.Thr375=
XM_005254943.1:c.1125T>A	XP_005255000.1:p.Thr375=
XR_243210.2:n.1228T>A
XR_429464.2:n.1228T>A
XR_931862.1:n.1228T>A
XR_931863.1:n.1228T>A
XR_931864.1:n.1228T>A
NM_001352507.1:c.378T>A	NP_001339436.1:p.Thr126=
NM_001352508.1:c.1080T>A	NP_001339437.1:p.Thr360=
NR_148017.1:n.1348T>A
NR_148018.1:n.1348T>A
NR_148019.1:n.1352T>A
XM_005254941.2:c.1125T>A	XP_005254998.1:p.Thr375=
XM_005254943.2:c.1125T>A	XP_005255000.1:p.Thr375=
XM_017022399.2:c.378T>A	XP_016877888.1:p.Thr126=
XM_017022400.2:c.378T>A	XP_016877889.1:p.Thr126=
XM_024449979.1:c.1125T>A	XP_024305747.1:p.Thr375=
XM_024449980.1:c.1125T>A	XP_024305748.1:p.Thr375=
XR_001751346.2:n.2140T>A
XR_001751347.2:n.2140T>A
XR_001751348.2:n.2140T>A
XR_002957655.1:n.2140T>A
XR_931862.3:n.2140T>A
NM_001040616.3:c.1125T>A MANE Select	NP_001035706.2:p.Thr375=
NM_001352507.2:c.378T>A	NP_001339436.1:p.Thr126=
NM_001352508.2:c.1080T>A	NP_001339437.1:p.Thr360=
NR_148017.2:n.1292T>A
NR_148018.2:n.1292T>A
NR_148019.2:n.1296T>A