Canonical Allele Identifier: CA260561342

Gene: LGALS3

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.55138318_55138320delinsCCT , CM000676.2:g.55138318_55138320delinsCCT	GRCh38
NC_000014.8:g.55605036_55605038delinsCCT , CM000676.1:g.55605036_55605038delinsCCT	GRCh37
NC_000014.7:g.54674789_54674791delinsCCT	NCBI36
NG_017089.1:g.14102_14104delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254301.14:c.292_294delinsCCT MANE Select	ENSP00000254301.9:p.Thr98Pro
ENST00000254301.13:c.292_294delinsCCT	ENSP00000254301.9:p.Thr98Pro
ENST00000553755.5:n.319_321delinsCCT
ENST00000554715.1:c.292_294delinsCCT	ENSP00000451381.1:p.Thr98Pro
ENST00000556263.1:n.275_277delinsCCT
ENST00000556322.1:n.365_367delinsCCT
ENST00000556438.6:n.1131_1133delinsCCT
NM_001177388.1:c.292_294delinsCCT	NP_001170859.1:p.Thr98Pro
NM_002306.3:c.292_294delinsCCT	NP_002297.2:p.Thr98Pro
NR_003225.2:n.1336_1338delinsCCT
XM_011536759.1:c.292_294delinsCCT	XP_011535061.1:p.Thr98Pro
NM_001357678.1:c.334_336delinsCCT	NP_001344607.1:p.Thr112Pro
NM_002306.4:c.292_294delinsCCT MANE Select	NP_002297.2:p.Thr98Pro
NM_001357678.2:c.334_336delinsCCT	NP_001344607.1:p.Thr112Pro