Canonical Allele Identifier: CA2630620893

Gene: LINS1

Linked Data

• gnomAD v4: 15-100573611-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100573612del , CM000677.2:g.100573612del	GRCh38
NC_000015.9:g.101113817del , CM000677.1:g.101113817del	GRCh37
NC_000015.8:g.98931340del	NCBI36
NG_034076.1:g.33629del
NG_034076.2:g.34421del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314742.13:c.1222+39del MANE Select	ENSP00000318423.8:n.1222+39del
ENST00000314742.12:c.1222+39del	ENSP00000318423.8:n.1222+39del
ENST00000559149.5:n.1379+39del
ENST00000560133.5:c.904del	ENSP00000454929.1:p.Ile302PhefsTer3
ENST00000560783.1:c.191+39del
ENST00000561308.5:c.1261del	ENSP00000454200.1:p.Ile421PhefsTer3
NM_001040616.2:c.1222+39del	NP_001035706.1:n.1222+39del
XM_005254941.1:c.1222+39del	XP_005254998.1:n.1222+39del
XM_005254943.1:c.1222+39del	XP_005255000.1:n.1222+39del
XR_243210.2:n.1325+39del
XR_429464.2:n.1325+39del
XR_931862.1:n.1325+39del
XR_931863.1:n.1325+39del
XR_931864.1:n.1325+39del
NM_001352507.1:c.475+39del	NP_001339436.1:n.475+39del
NM_001352508.1:c.1177+39del	NP_001339437.1:n.1177+39del
NR_148017.1:n.1445+39del
NR_148018.1:n.1445+39del
NR_148019.1:n.1449+39del
XM_005254941.2:c.1222+39del	XP_005254998.1:n.1222+39del
XM_005254943.2:c.1222+39del	XP_005255000.1:n.1222+39del
XM_017022399.2:c.475+39del	XP_016877888.1:n.475+39del
XM_017022400.2:c.475+39del	XP_016877889.1:n.475+39del
XM_024449979.1:c.1222+39del	XP_024305747.1:n.1222+39del
XM_024449980.1:c.1222+39del	XP_024305748.1:n.1222+39del
XR_001751346.2:n.2237+39del
XR_001751347.2:n.2237+39del
XR_001751348.2:n.2237+39del
XR_002957655.1:n.2237+39del
XR_931862.3:n.2237+39del
NM_001040616.3:c.1222+39del MANE Select	NP_001035706.2:n.1222+39del
NM_001352507.2:c.475+39del	NP_001339436.1:n.475+39del
NM_001352508.2:c.1177+39del	NP_001339437.1:n.1177+39del
NR_148017.2:n.1389+39del
NR_148018.2:n.1389+39del
NR_148019.2:n.1393+39del