Canonical Allele Identifier: CA2138356472

Gene: LGALS3

Linked Data

• dbSNP Id: rs1881390501

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.55136230_55136258del , CM000676.2:g.55136230_55136258del	GRCh38
NC_000014.8:g.55602948_55602976del , CM000676.1:g.55602948_55602976del	GRCh37
NC_000014.7:g.54672701_54672729del	NCBI36
NG_017089.1:g.12014_12042del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254301.14:c.-4-1140_-4-1112del MANE Select	ENSP00000254301.9:n.-4-1140_-4-1112del
ENST00000254301.13:c.-4-1140_-4-1112del	ENSP00000254301.9:n.-4-1140_-4-1112del
ENST00000553493.5:c.-4-1140_-4-1112del	ENSP00000451526.1:n.-4-1140_-4-1112del
ENST00000553755.5:n.46-1815_46-1787del
ENST00000554715.1:c.-4-1140_-4-1112del	ENSP00000451381.1:n.-4-1140_-4-1112del
NM_001177388.1:c.-4-1140_-4-1112del	NP_001170859.1:n.-4-1140_-4-1112del
NM_002306.3:c.-4-1140_-4-1112del	NP_002297.2:n.-4-1140_-4-1112del
XM_011536759.1:c.-4-1140_-4-1112del	XP_011535061.1:n.-4-1140_-4-1112del
NM_001357678.1:c.39-1140_39-1112del	NP_001344607.1:n.39-1140_39-1112del
NM_002306.4:c.-4-1140_-4-1112del MANE Select	NP_002297.2:n.-4-1140_-4-1112del
NM_001357678.2:c.39-1140_39-1112del	NP_001344607.1:n.39-1140_39-1112del