Canonical Allele Identifier: CA2138359055
Community Standard Title: NM_002306.4(LGALS3):c.191C= (p.Pro64=)
Gene: LGALS3 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_002306.4:c.191C= MANE Select NP_002297.2:p.Pro64=
ENST00000254301.14:c.191C= MANE Select ENSP00000254301.9:p.Pro64=
NM_001177388.1:c.191C= NP_001170859.1:p.Pro64=
NM_001357678.1:c.233C= NP_001344607.1:p.Pro78=
NM_001357678.2:c.233C= NP_001344607.1:p.Pro78=
NM_002306.3:c.191C= NP_002297.2:p.Pro64=
NR_003225.2:n.1235C=
ENST00000254301.13:c.191C= ENSP00000254301.9:p.Pro64=
ENST00000553493.5:c.191C= ENSP00000451526.1:p.Pro64=
ENST00000553755.5:n.218C=
ENST00000554715.1:c.191C= ENSP00000451381.1:p.Pro64=
ENST00000556263.1:n.174C=
ENST00000556322.1:n.264C=
ENST00000556438.6:n.1030C=
XM_011536759.1:c.191C= XP_011535061.1:p.Pro64=