Canonical Allele Identifier: CA963360981
Gene: LGALS3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.55136322_55136323del , CM000676.2:g.55136322_55136323del GRCh38
NC_000014.8:g.55603040_55603041del , CM000676.1:g.55603040_55603041del GRCh37
NC_000014.7:g.54672793_54672794del NCBI36
NG_017089.1:g.12106_12107del

Transcript Alleles

HGVS Amino-acid change
ENST00000254301.14:c.-4-1048_-4-1047del MANE Select ENSP00000254301.9:n.-4-1048_-4-1047del
ENST00000254301.13:c.-4-1048_-4-1047del ENSP00000254301.9:n.-4-1048_-4-1047del
ENST00000553493.5:c.-4-1048_-4-1047del ENSP00000451526.1:n.-4-1048_-4-1047del
ENST00000553755.5:n.46-1723_46-1722del
ENST00000554715.1:c.-4-1048_-4-1047del ENSP00000451381.1:n.-4-1048_-4-1047del
NM_001177388.1:c.-4-1048_-4-1047del NP_001170859.1:n.-4-1048_-4-1047del
NM_002306.3:c.-4-1048_-4-1047del NP_002297.2:n.-4-1048_-4-1047del
XM_011536759.1:c.-4-1048_-4-1047del XP_011535061.1:n.-4-1048_-4-1047del
NM_001357678.1:c.39-1048_39-1047del NP_001344607.1:n.39-1048_39-1047del
NM_002306.4:c.-4-1048_-4-1047del MANE Select NP_002297.2:n.-4-1048_-4-1047del
NM_001357678.2:c.39-1048_39-1047del NP_001344607.1:n.39-1048_39-1047del