Canonical Allele Identifier: CA614290802

Gene: LGALS3

Linked Data

• dbSNP Id: rs1369773686
• gnomAD v2: 14-55603106-GAAGT-G
• gnomAD v3: 14-55136388-GAAGT-G
• gnomAD v4: 14-55136388-GAAGT-G
• MyVariant Identifiers: chr14:g.55603107_55603110del (hg19) ; chr14:g.55136389_55136392del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.55136392_55136395del , CM000676.2:g.55136392_55136395del	GRCh38
NC_000014.8:g.55603110_55603113del , CM000676.1:g.55603110_55603113del	GRCh37
NC_000014.7:g.54672863_54672866del	NCBI36
NG_017089.1:g.12176_12179del

Transcript Alleles

HGVS	Amino-acid change
ENST00000254301.14:c.-4-978_-4-975del MANE Select	ENSP00000254301.9:n.-4-978_-4-975del
ENST00000254301.13:c.-4-978_-4-975del	ENSP00000254301.9:n.-4-978_-4-975del
ENST00000553493.5:c.-4-978_-4-975del	ENSP00000451526.1:n.-4-978_-4-975del
ENST00000553755.5:n.46-1653_46-1650del
ENST00000554715.1:c.-4-978_-4-975del	ENSP00000451381.1:n.-4-978_-4-975del
NM_001177388.1:c.-4-978_-4-975del	NP_001170859.1:n.-4-978_-4-975del
NM_002306.3:c.-4-978_-4-975del	NP_002297.2:n.-4-978_-4-975del
XM_011536759.1:c.-4-978_-4-975del	XP_011535061.1:n.-4-978_-4-975del
NM_001357678.1:c.39-978_39-975del	NP_001344607.1:n.39-978_39-975del
NM_002306.4:c.-4-978_-4-975del MANE Select	NP_002297.2:n.-4-978_-4-975del
NM_001357678.2:c.39-978_39-975del	NP_001344607.1:n.39-978_39-975del