Canonical Allele Identifier: CA5928778
Community Standard Title: NM_018490.5(LGR4):c.286A>G (p.Ile96Val)
Gene: LGR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27392490T>C , CM000673.2:g.27392490T>C GRCh38
NC_000011.9:g.27414037T>C , CM000673.1:g.27414037T>C GRCh37
NC_000011.8:g.27370613T>C NCBI36
NG_051818.1:g.85286A>G

Transcript Alleles

HGVS Amino-acid Change
NM_018490.5:c.286A>G MANE Select NP_060960.2:p.Ile96Val
ENST00000379214.9:c.286A>G MANE Select ENSP00000368516.4:p.Ile96Val
NM_001346432.1:c.214A>G NP_001333361.1:p.Ile72Val
NM_001346432.2:c.214A>G NP_001333361.1:p.Ile72Val
NM_018490.2:c.286A>G NP_060960.2:p.Ile96Val
NM_018490.3:c.286A>G NP_060960.2:p.Ile96Val
NM_018490.4:c.286A>G NP_060960.2:p.Ile96Val
ENST00000379214.8:c.286A>G ENSP00000368516.4:p.Ile96Val
ENST00000389858.4:c.214A>G ENSP00000374508.4:p.Ile72Val
ENST00000480977.2:c.258-7022A>G ENSP00000431650.1:n.258-7022A>G