Canonical Allele Identifier: CA144010
Community Standard Title: NM_018490.5(LGR4):c.376C>T (p.Arg126Ter)
Gene: LGR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27391119G>A , CM000673.2:g.27391119G>A GRCh38
NC_000011.9:g.27412666G>A , CM000673.1:g.27412666G>A GRCh37
NC_000011.8:g.27369242G>A NCBI36
NG_051818.1:g.86657C>T

Transcript Alleles

HGVS Amino-acid Change
NM_018490.5:c.376C>T MANE Select NP_060960.2:p.Arg126Ter
ENST00000379214.9:c.376C>T MANE Select ENSP00000368516.4:p.Arg126Ter
NM_001346432.1:c.304C>T NP_001333361.1:p.Arg102Ter
NM_001346432.2:c.304C>T NP_001333361.1:p.Arg102Ter
NM_018490.2:c.376C>T NP_060960.2:p.Arg126Ter
NM_018490.3:c.376C>T NP_060960.2:p.Arg126Ter
NM_018490.4:c.376C>T NP_060960.2:p.Arg126Ter
ENST00000379214.8:c.376C>T ENSP00000368516.4:p.Arg126Ter
ENST00000389858.4:c.304C>T ENSP00000374508.4:p.Arg102Ter
ENST00000480977.2:c.258-5651C>T ENSP00000431650.1:n.258-5651C>T