Canonical Allele Identifier: CA2275574366

Gene: LLGL2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75568858_75568859delinsAC , CM000679.2:g.75568858_75568859delinsAC	GRCh38
NC_000017.10:g.73564939_73564940delinsAC , CM000679.1:g.73564939_73564940delinsAC	GRCh37
NC_000017.9:g.71076534_71076535delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392550.8:c.1322+19_1322+20delinsAC MANE Select	ENSP00000376333.4:n.1322+19_1322+20delinsAC
ENST00000167462.9:c.1322+19_1322+20delinsAC	ENSP00000167462.5:n.1322+19_1322+20delinsAC
ENST00000392550.7:c.1322+19_1322+20delinsAC	ENSP00000376333.3:n.1322+19_1322+20delinsAC
ENST00000545227.6:n.1499+19_1499+20delinsAC
ENST00000577200.5:c.1322+19_1322+20delinsAC	ENSP00000464397.1:n.1322+19_1322+20delinsAC
ENST00000577500.5:n.842+19_842+20delinsAC
ENST00000578638.5:c.313+19_313+20delinsAC
ENST00000578719.1:c.22+19_22+20delinsAC
NM_001031803.1:c.1322+19_1322+20delinsAC	NP_001026973.1:n.1322+19_1322+20delinsAC
NM_004524.2:c.1322+19_1322+20delinsAC	NP_004515.2:n.1322+19_1322+20delinsAC
XM_006721897.2:c.1322+19_1322+20delinsAC	XP_006721960.1:n.1322+19_1322+20delinsAC
XM_011524801.1:c.1322+19_1322+20delinsAC	XP_011523103.1:n.1322+19_1322+20delinsAC
XM_011524802.1:c.1322+19_1322+20delinsAC	XP_011523104.1:n.1322+19_1322+20delinsAC
XM_011524803.1:c.1322+19_1322+20delinsAC	XP_011523105.1:n.1322+19_1322+20delinsAC
XM_011524804.1:c.1322+19_1322+20delinsAC	XP_011523106.1:n.1322+19_1322+20delinsAC
XM_011524805.1:c.1322+19_1322+20delinsAC	XP_011523107.1:n.1322+19_1322+20delinsAC
XM_011524806.1:c.1322+19_1322+20delinsAC	XP_011523108.1:n.1322+19_1322+20delinsAC
XM_011524807.1:c.1124+19_1124+20delinsAC	XP_011523109.1:n.1124+19_1124+20delinsAC
XM_017024625.1:c.1322+19_1322+20delinsAC	XP_016880114.1:n.1322+19_1322+20delinsAC
XM_017024626.1:c.1322+19_1322+20delinsAC	XP_016880115.1:n.1322+19_1322+20delinsAC
XM_017024627.1:c.1322+19_1322+20delinsAC	XP_016880116.1:n.1322+19_1322+20delinsAC
XM_017024628.1:c.1322+19_1322+20delinsAC	XP_016880117.1:n.1322+19_1322+20delinsAC
XM_017024629.1:c.1322+19_1322+20delinsAC	XP_016880118.1:n.1322+19_1322+20delinsAC
XM_017024630.1:c.1322+19_1322+20delinsAC	XP_016880119.1:n.1322+19_1322+20delinsAC
XM_017024631.1:c.1322+19_1322+20delinsAC	XP_016880120.1:n.1322+19_1322+20delinsAC
XR_001752508.1:n.1447+19_1447+20delinsAC
XR_002957999.1:n.1447+19_1447+20delinsAC
XR_002958000.1:n.1514+19_1514+20delinsAC
XR_002958001.1:n.1557+19_1557+20delinsAC
XR_002958002.1:n.1486+19_1486+20delinsAC
XR_002958003.1:n.1447+19_1447+20delinsAC
XR_002958004.1:n.1565+19_1565+20delinsAC
XR_002958005.1:n.1583+19_1583+20delinsAC
NM_001031803.2:c.1322+19_1322+20delinsAC MANE Select	NP_001026973.1:n.1322+19_1322+20delinsAC
NM_004524.3:c.1322+19_1322+20delinsAC	NP_004515.2:n.1322+19_1322+20delinsAC