Canonical Allele Identifier: CA963360983
Gene: LGALS3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.55136318_55136323dup , CM000676.2:g.55136318_55136323dup GRCh38
NC_000014.8:g.55603036_55603041dup , CM000676.1:g.55603036_55603041dup GRCh37
NC_000014.7:g.54672789_54672794dup NCBI36
NG_017089.1:g.12102_12107dup

Transcript Alleles

HGVS Amino-acid change
ENST00000254301.14:c.-4-1052_-4-1047dup MANE Select ENSP00000254301.9:n.-4-1052_-4-1047dup
ENST00000254301.13:c.-4-1052_-4-1047dup ENSP00000254301.9:n.-4-1052_-4-1047dup
ENST00000553493.5:c.-4-1052_-4-1047dup ENSP00000451526.1:n.-4-1052_-4-1047dup
ENST00000553755.5:n.46-1727_46-1722dup
ENST00000554715.1:c.-4-1052_-4-1047dup ENSP00000451381.1:n.-4-1052_-4-1047dup
NM_001177388.1:c.-4-1052_-4-1047dup NP_001170859.1:n.-4-1052_-4-1047dup
NM_002306.3:c.-4-1052_-4-1047dup NP_002297.2:n.-4-1052_-4-1047dup
XM_011536759.1:c.-4-1052_-4-1047dup XP_011535061.1:n.-4-1052_-4-1047dup
NM_001357678.1:c.39-1052_39-1047dup NP_001344607.1:n.39-1052_39-1047dup
NM_002306.4:c.-4-1052_-4-1047dup MANE Select NP_002297.2:n.-4-1052_-4-1047dup
NM_001357678.2:c.39-1052_39-1047dup NP_001344607.1:n.39-1052_39-1047dup