Canonical Allele Identifier: CA389792569

Gene: LGALS3

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.55138217C>G , CM000676.2:g.55138217C>G	GRCh38
NC_000014.8:g.55604935C>G , CM000676.1:g.55604935C>G	GRCh37
NC_000014.7:g.54674688C>G	NCBI36
NG_017089.1:g.14001C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254301.14:c.191C>G MANE Select	ENSP00000254301.9:p.Pro64Arg
ENST00000254301.13:c.191C>G	ENSP00000254301.9:p.Pro64Arg
ENST00000553493.5:c.191C>G	ENSP00000451526.1:p.Pro64Arg
ENST00000553755.5:n.218C>G
ENST00000554715.1:c.191C>G	ENSP00000451381.1:p.Pro64Arg
ENST00000556263.1:n.174C>G
ENST00000556322.1:n.264C>G
ENST00000556438.6:n.1030C>G
NM_001177388.1:c.191C>G	NP_001170859.1:p.Pro64Arg
NM_002306.3:c.191C>G	NP_002297.2:p.Pro64Arg
NR_003225.2:n.1235C>G
XM_011536759.1:c.191C>G	XP_011535061.1:p.Pro64Arg
NM_001357678.1:c.233C>G	NP_001344607.1:p.Pro78Arg
NM_002306.4:c.191C>G MANE Select	NP_002297.2:p.Pro64Arg
NM_001357678.2:c.233C>G	NP_001344607.1:p.Pro78Arg