Canonical Allele Identifier: CA2200116465

Gene: LINS1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100573649_100573654delinsACCTTT , CM000677.2:g.100573649_100573654delinsACCTTT	GRCh38
NC_000015.9:g.101113854_101113859delinsACCTTT , CM000677.1:g.101113854_101113859delinsACCTTT	GRCh37
NC_000015.8:g.98931377_98931382delinsACCTTT	NCBI36
NG_034076.1:g.33587_33592delinsAAAGGT
NG_034076.2:g.34379_34384delinsAAAGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314742.13:c.1219_1222+2delinsAAAGGT
ENST00000314742.12:c.1219_1222+2delinsAAAGGT
ENST00000559149.5:n.1376_1379+2delinsAAAGGT
ENST00000560133.5:c.862_867delinsAAAGGT	ENSP00000454929.1:p.Lys288=
ENST00000560783.1:c.188_191+2delinsAAAGGT
ENST00000561308.5:c.1219_1224delinsAAAGGT	ENSP00000454200.1:p.Lys407=
NM_001040616.2:c.1219_1222+2delinsAAAGGT
XM_005254941.1:c.1219_1222+2delinsAAAGGT
XM_005254943.1:c.1219_1222+2delinsAAAGGT
XR_243210.2:n.1322_1325+2delinsAAAGGT
XR_429464.2:n.1322_1325+2delinsAAAGGT
XR_931862.1:n.1322_1325+2delinsAAAGGT
XR_931863.1:n.1322_1325+2delinsAAAGGT
XR_931864.1:n.1322_1325+2delinsAAAGGT
NM_001352507.1:c.472_475+2delinsAAAGGT
NM_001352508.1:c.1174_1177+2delinsAAAGGT
NR_148017.1:n.1442_1445+2delinsAAAGGT
NR_148018.1:n.1442_1445+2delinsAAAGGT
NR_148019.1:n.1446_1449+2delinsAAAGGT
XM_005254941.2:c.1219_1222+2delinsAAAGGT
XM_005254943.2:c.1219_1222+2delinsAAAGGT
XM_017022399.2:c.472_475+2delinsAAAGGT
XM_017022400.2:c.472_475+2delinsAAAGGT
XM_024449979.1:c.1219_1222+2delinsAAAGGT
XM_024449980.1:c.1219_1222+2delinsAAAGGT
XR_001751346.2:n.2234_2237+2delinsAAAGGT
XR_001751347.2:n.2234_2237+2delinsAAAGGT
XR_001751348.2:n.2234_2237+2delinsAAAGGT
XR_002957655.1:n.2234_2237+2delinsAAAGGT
XR_931862.3:n.2234_2237+2delinsAAAGGT
NM_001040616.3:c.1219_1222+2delinsAAAGGT
NM_001352507.2:c.472_475+2delinsAAAGGT
NM_001352508.2:c.1174_1177+2delinsAAAGGT
NR_148017.2:n.1386_1389+2delinsAAAGGT
NR_148018.2:n.1386_1389+2delinsAAAGGT
NR_148019.2:n.1390_1393+2delinsAAAGGT