Canonical Allele Identifier: CA620301518

Gene: LINS1

Linked Data

• dbSNP Id: rs1190895700
• gnomAD v2: 15-101113810-AAGT-A
• gnomAD v3: 15-100573605-AAGT-A
• gnomAD v4: 15-100573605-AAGT-A
• MyVariant Identifiers: chr15:g.101113811_101113813del (hg19) ; chr15:g.100573606_100573608del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100573607_100573609del , CM000677.2:g.100573607_100573609del	GRCh38
NC_000015.9:g.101113812_101113814del , CM000677.1:g.101113812_101113814del	GRCh37
NC_000015.8:g.98931335_98931337del	NCBI36
NG_034076.1:g.33633_33635del
NG_034076.2:g.34425_34427del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314742.13:c.1222+43_1222+45del MANE Select	ENSP00000318423.8:n.1222+43_1222+45del
ENST00000314742.12:c.1222+43_1222+45del	ENSP00000318423.8:n.1222+43_1222+45del
ENST00000559149.5:n.1379+43_1379+45del
ENST00000560133.5:c.908_910del	ENSP00000454929.1:p.Tyr303del
ENST00000560783.1:c.191+43_191+45del
ENST00000561308.5:c.1265_1267del	ENSP00000454200.1:p.Tyr422del
NM_001040616.2:c.1222+43_1222+45del	NP_001035706.1:n.1222+43_1222+45del
XM_005254941.1:c.1222+43_1222+45del	XP_005254998.1:n.1222+43_1222+45del
XM_005254943.1:c.1222+43_1222+45del	XP_005255000.1:n.1222+43_1222+45del
XR_243210.2:n.1325+43_1325+45del
XR_429464.2:n.1325+43_1325+45del
XR_931862.1:n.1325+43_1325+45del
XR_931863.1:n.1325+43_1325+45del
XR_931864.1:n.1325+43_1325+45del
NM_001352507.1:c.475+43_475+45del	NP_001339436.1:n.475+43_475+45del
NM_001352508.1:c.1177+43_1177+45del	NP_001339437.1:n.1177+43_1177+45del
NR_148017.1:n.1445+43_1445+45del
NR_148018.1:n.1445+43_1445+45del
NR_148019.1:n.1449+43_1449+45del
XM_005254941.2:c.1222+43_1222+45del	XP_005254998.1:n.1222+43_1222+45del
XM_005254943.2:c.1222+43_1222+45del	XP_005255000.1:n.1222+43_1222+45del
XM_017022399.2:c.475+43_475+45del	XP_016877888.1:n.475+43_475+45del
XM_017022400.2:c.475+43_475+45del	XP_016877889.1:n.475+43_475+45del
XM_024449979.1:c.1222+43_1222+45del	XP_024305747.1:n.1222+43_1222+45del
XM_024449980.1:c.1222+43_1222+45del	XP_024305748.1:n.1222+43_1222+45del
XR_001751346.2:n.2237+43_2237+45del
XR_001751347.2:n.2237+43_2237+45del
XR_001751348.2:n.2237+43_2237+45del
XR_002957655.1:n.2237+43_2237+45del
XR_931862.3:n.2237+43_2237+45del
NM_001040616.3:c.1222+43_1222+45del MANE Select	NP_001035706.2:n.1222+43_1222+45del
NM_001352507.2:c.475+43_475+45del	NP_001339436.1:n.475+43_475+45del
NM_001352508.2:c.1177+43_1177+45del	NP_001339437.1:n.1177+43_1177+45del
NR_148017.2:n.1389+43_1389+45del
NR_148018.2:n.1389+43_1389+45del
NR_148019.2:n.1393+43_1393+45del