Canonical Allele Identifier: CA2138356629

Gene: LGALS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.55136369_55136374delinsACCTTT , CM000676.2:g.55136369_55136374delinsACCTTT	GRCh38
NC_000014.8:g.55603087_55603092delinsACCTTT , CM000676.1:g.55603087_55603092delinsACCTTT	GRCh37
NC_000014.7:g.54672840_54672845delinsACCTTT	NCBI36
NG_017089.1:g.12153_12158delinsACCTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000254301.14:c.-4-1001_-4-996delinsACCTTT MANE Select	ENSP00000254301.9:n.-4-1001_-4-996delinsACCTTT
ENST00000254301.13:c.-4-1001_-4-996delinsACCTTT	ENSP00000254301.9:n.-4-1001_-4-996delinsACCTTT
ENST00000553493.5:c.-4-1001_-4-996delinsACCTTT	ENSP00000451526.1:n.-4-1001_-4-996delinsACCTTT
ENST00000553755.5:n.46-1676_46-1671delinsACCTTT
ENST00000554715.1:c.-4-1001_-4-996delinsACCTTT	ENSP00000451381.1:n.-4-1001_-4-996delinsACCTTT
NM_001177388.1:c.-4-1001_-4-996delinsACCTTT	NP_001170859.1:n.-4-1001_-4-996delinsACCTTT
NM_002306.3:c.-4-1001_-4-996delinsACCTTT	NP_002297.2:n.-4-1001_-4-996delinsACCTTT
XM_011536759.1:c.-4-1001_-4-996delinsACCTTT	XP_011535061.1:n.-4-1001_-4-996delinsACCTTT
NM_001357678.1:c.39-1001_39-996delinsACCTTT	NP_001344607.1:n.39-1001_39-996delinsACCTTT
NM_002306.4:c.-4-1001_-4-996delinsACCTTT MANE Select	NP_002297.2:n.-4-1001_-4-996delinsACCTTT
NM_001357678.2:c.39-1001_39-996delinsACCTTT	NP_001344607.1:n.39-1001_39-996delinsACCTTT