Canonical Allele Identifier: CA2275574480

Gene: LLGL2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75569090T= , CM000679.2:g.75569090T=	GRCh38
NC_000017.10:g.73565171T= , CM000679.1:g.73565171T=	GRCh37
NC_000017.9:g.71076766T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000392550.8:c.1435T= MANE Select	ENSP00000376333.4:p.Phe479=
ENST00000167462.9:c.1435T=	ENSP00000167462.5:p.Phe479=
ENST00000392550.7:c.1435T=	ENSP00000376333.3:p.Phe479=
ENST00000545227.6:n.1612T=
ENST00000577200.5:c.1435T=	ENSP00000464397.1:p.Phe479=
ENST00000577500.5:n.955T=
ENST00000578638.5:c.426T=
ENST00000578719.1:c.152T=
NM_001031803.1:c.1435T=	NP_001026973.1:p.Phe479=
NM_004524.2:c.1435T=	NP_004515.2:p.Phe479=
XM_006721897.2:c.1435T=	XP_006721960.1:p.Phe479=
XM_011524801.1:c.1435T=	XP_011523103.1:p.Phe479=
XM_011524802.1:c.1435T=	XP_011523104.1:p.Phe479=
XM_011524803.1:c.1435T=	XP_011523105.1:p.Phe479=
XM_011524804.1:c.1435T=	XP_011523106.1:p.Phe479=
XM_011524805.1:c.1435T=	XP_011523107.1:p.Phe479=
XM_011524806.1:c.1435T=	XP_011523108.1:p.Phe479=
XM_011524807.1:c.1237T=	XP_011523109.1:p.Phe413=
XM_017024625.1:c.1435T=	XP_016880114.1:p.Phe479=
XM_017024626.1:c.1435T=	XP_016880115.1:p.Phe479=
XM_017024627.1:c.1435T=	XP_016880116.1:p.Phe479=
XM_017024628.1:c.1435T=	XP_016880117.1:p.Phe479=
XM_017024629.1:c.1435T=	XP_016880118.1:p.Phe479=
XM_017024630.1:c.1435T=	XP_016880119.1:p.Phe479=
XM_017024631.1:c.1435T=	XP_016880120.1:p.Phe479=
XR_001752508.1:n.1560T=
XR_002957999.1:n.1560T=
XR_002958000.1:n.1627T=
XR_002958001.1:n.1670T=
XR_002958002.1:n.1599T=
XR_002958003.1:n.1560T=
XR_002958004.1:n.1678T=
XR_002958005.1:n.1696T=
NM_001031803.2:c.1435T= MANE Select	NP_001026973.1:p.Phe479=
NM_004524.3:c.1435T=	NP_004515.2:p.Phe479=