Canonical Allele Identifier: CA289045057

Gene: LGALS9

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27640666A>G , CM000679.2:g.27640666A>G	GRCh38
NC_000017.10:g.25967692A>G , CM000679.1:g.25967692A>G	GRCh37
NC_000017.9:g.22991819A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_009587.3:c.226A>G MANE Select	NP_033665.1:p.Thr76Ala
ENST00000395473.7:c.226A>G MANE Select	ENSP00000378856.2:p.Thr76Ala
NM_001330163.1:c.226A>G	NP_001317092.1:p.Thr76Ala
NM_001330163.2:c.226A>G	NP_001317092.1:p.Thr76Ala
NM_002308.3:c.226A>G	NP_002299.2:p.Thr76Ala
NM_002308.4:c.226A>G	NP_002299.2:p.Thr76Ala
NM_009587.2:c.226A>G	NP_033665.1:p.Thr76Ala
NR_024043.1:n.273A>G
NR_024043.2:n.233A>G
ENST00000302228.9:c.226A>G	ENSP00000306228.5:p.Thr76Ala
ENST00000313648.10:c.226A>G	ENSP00000318214.6:p.Thr76Ala
ENST00000395473.6:c.226A>G	ENSP00000378856.2:p.Thr76Ala
ENST00000448970.6:n.283A>G
ENST00000467111.5:c.155A>G	ENSP00000462668.1:p.His52Arg
ENST00000577392.5:c.226A>G	ENSP00000462359.1:p.Thr76Ala
ENST00000579930.5:n.304A>G
ENST00000580779.5:c.155A>G	ENSP00000463125.1:p.His52Arg
ENST00000583671.1:n.280A>G
ENST00000584386.5:n.266A>G
ENST00000584605.5:c.492A>G	ENSP00000463557.1:n.492A>G
ENST00000584661.5:c.-45A>G	ENSP00000467505.1:n.-45A>G
XM_006721892.1:c.226A>G	XP_006721955.1:p.Thr76Ala
XM_006721892.3:c.226A>G	XP_006721955.1:p.Thr76Ala
XM_006721893.2:c.226A>G	XP_006721956.1:p.Thr76Ala
XM_006721893.3:c.226A>G	XP_006721956.1:p.Thr76Ala
XM_006721894.2:c.226A>G	XP_006721957.1:p.Thr76Ala
XM_006721895.2:c.226A>G	XP_006721958.1:p.Thr76Ala
XM_006721895.4:c.226A>G	XP_006721958.1:p.Thr76Ala
XM_011524796.1:c.226A>G	XP_011523098.1:p.Thr76Ala
XM_011524796.2:c.226A>G	XP_011523098.1:p.Thr76Ala
XM_017024623.2:c.226A>G	XP_016880112.1:p.Thr76Ala