Canonical Allele Identifier: CA614290797

Gene: LGALS3

Linked Data

• dbSNP Id: rs1278841781
• gnomAD v2: 14-55602890-T-A
• gnomAD v3: 14-55136172-T-A
• gnomAD v4: 14-55136172-T-A
• MyVariant Identifiers: chr14:g.55602890T>A (hg19) ; chr14:g.55136172T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.55136172T>A , CM000676.2:g.55136172T>A	GRCh38
NC_000014.8:g.55602890T>A , CM000676.1:g.55602890T>A	GRCh37
NC_000014.7:g.54672643T>A	NCBI36
NG_017089.1:g.11956T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000254301.14:c.-4-1198T>A MANE Select	ENSP00000254301.9:n.-4-1198T>A
ENST00000254301.13:c.-4-1198T>A	ENSP00000254301.9:n.-4-1198T>A
ENST00000553493.5:c.-4-1198T>A	ENSP00000451526.1:n.-4-1198T>A
ENST00000553755.5:n.46-1873T>A
ENST00000554715.1:c.-4-1198T>A	ENSP00000451381.1:n.-4-1198T>A
NM_001177388.1:c.-4-1198T>A	NP_001170859.1:n.-4-1198T>A
NM_002306.3:c.-4-1198T>A	NP_002297.2:n.-4-1198T>A
XM_011536759.1:c.-4-1198T>A	XP_011535061.1:n.-4-1198T>A
NM_001357678.1:c.39-1198T>A	NP_001344607.1:n.39-1198T>A
NM_002306.4:c.-4-1198T>A MANE Select	NP_002297.2:n.-4-1198T>A
NM_001357678.2:c.39-1198T>A	NP_001344607.1:n.39-1198T>A