Canonical Allele Identifier: CA401032968

Gene: LLGL2

Linked Data

• MyVariant Identifiers: chr17:g.73565062C>A (hg19) ; chr17:g.75568981C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75568981C>A , CM000679.2:g.75568981C>A	GRCh38
NC_000017.10:g.73565062C>A , CM000679.1:g.73565062C>A	GRCh37
NC_000017.9:g.71076657C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392550.8:c.1326C>A MANE Select	ENSP00000376333.4:p.His442Gln
ENST00000167462.9:c.1326C>A	ENSP00000167462.5:p.His442Gln
ENST00000392550.7:c.1326C>A	ENSP00000376333.3:p.His442Gln
ENST00000545227.6:n.1503C>A
ENST00000577200.5:c.1326C>A	ENSP00000464397.1:p.His442Gln
ENST00000577500.5:n.846C>A
ENST00000578638.5:c.317C>A
ENST00000578719.1:c.43C>A
NM_001031803.1:c.1326C>A	NP_001026973.1:p.His442Gln
NM_004524.2:c.1326C>A	NP_004515.2:p.His442Gln
XM_006721897.2:c.1326C>A	XP_006721960.1:p.His442Gln
XM_011524801.1:c.1326C>A	XP_011523103.1:p.His442Gln
XM_011524802.1:c.1326C>A	XP_011523104.1:p.His442Gln
XM_011524803.1:c.1326C>A	XP_011523105.1:p.His442Gln
XM_011524804.1:c.1326C>A	XP_011523106.1:p.His442Gln
XM_011524805.1:c.1326C>A	XP_011523107.1:p.His442Gln
XM_011524806.1:c.1326C>A	XP_011523108.1:p.His442Gln
XM_011524807.1:c.1128C>A	XP_011523109.1:p.His376Gln
XM_017024625.1:c.1326C>A	XP_016880114.1:p.His442Gln
XM_017024626.1:c.1326C>A	XP_016880115.1:p.His442Gln
XM_017024627.1:c.1326C>A	XP_016880116.1:p.His442Gln
XM_017024628.1:c.1326C>A	XP_016880117.1:p.His442Gln
XM_017024629.1:c.1326C>A	XP_016880118.1:p.His442Gln
XM_017024630.1:c.1326C>A	XP_016880119.1:p.His442Gln
XM_017024631.1:c.1326C>A	XP_016880120.1:p.His442Gln
XR_001752508.1:n.1451C>A
XR_002957999.1:n.1451C>A
XR_002958000.1:n.1518C>A
XR_002958001.1:n.1561C>A
XR_002958002.1:n.1490C>A
XR_002958003.1:n.1451C>A
XR_002958004.1:n.1569C>A
XR_002958005.1:n.1587C>A
NM_001031803.2:c.1326C>A MANE Select	NP_001026973.1:p.His442Gln
NM_004524.3:c.1326C>A	NP_004515.2:p.His442Gln