Canonical Allele Identifier: CA2138356459

Gene: LGALS3

Linked Data

• dbSNP Id: rs1881389958

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.55136200_55136201del , CM000676.2:g.55136200_55136201del	GRCh38
NC_000014.8:g.55602918_55602919del , CM000676.1:g.55602918_55602919del	GRCh37
NC_000014.7:g.54672671_54672672del	NCBI36
NG_017089.1:g.11984_11985del

Transcript Alleles

HGVS	Amino-acid change
ENST00000254301.14:c.-4-1170_-4-1169del MANE Select	ENSP00000254301.9:n.-4-1170_-4-1169del
ENST00000254301.13:c.-4-1170_-4-1169del	ENSP00000254301.9:n.-4-1170_-4-1169del
ENST00000553493.5:c.-4-1170_-4-1169del	ENSP00000451526.1:n.-4-1170_-4-1169del
ENST00000553755.5:n.46-1845_46-1844del
ENST00000554715.1:c.-4-1170_-4-1169del	ENSP00000451381.1:n.-4-1170_-4-1169del
NM_001177388.1:c.-4-1170_-4-1169del	NP_001170859.1:n.-4-1170_-4-1169del
NM_002306.3:c.-4-1170_-4-1169del	NP_002297.2:n.-4-1170_-4-1169del
XM_011536759.1:c.-4-1170_-4-1169del	XP_011535061.1:n.-4-1170_-4-1169del
NM_001357678.1:c.39-1170_39-1169del	NP_001344607.1:n.39-1170_39-1169del
NM_002306.4:c.-4-1170_-4-1169del MANE Select	NP_002297.2:n.-4-1170_-4-1169del
NM_001357678.2:c.39-1170_39-1169del	NP_001344607.1:n.39-1170_39-1169del