Canonical Allele Identifier: CA2136729262
Gene: FRMD6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.51610198_51610199delinsTG , CM000676.2:g.51610198_51610199delinsTG GRCh38
NC_000014.8:g.52076916_52076917delinsTG , CM000676.1:g.52076916_52076917delinsTG GRCh37
NC_000014.7:g.51146666_51146667delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356218.8:c.-147+39788_-147+39789delinsTG ENSP00000348550.4:n.-147+39788_-147+39789delinsTG
ENST00000554745.1:n.278-33254_278-33253delinsTG
ENST00000556137.5:n.508+39788_508+39789delinsTG
NM_001042481.2:c.-147+39788_-147+39789delinsTG NP_001035946.1:n.-147+39788_-147+39789delinsTG
XM_011536423.1:c.-147+39788_-147+39789delinsTG XP_011534725.1:n.-147+39788_-147+39789delinsTG
XM_011536424.1:c.-147+39788_-147+39789delinsTG XP_011534726.1:n.-147+39788_-147+39789delinsTG
XM_024449472.1:c.-147+39788_-147+39789delinsTG XP_024305240.1:n.-147+39788_-147+39789delinsTG
XM_024449473.1:c.-146-79493_-146-79492delinsTG XP_024305241.1:n.-146-79493_-146-79492delinsTG
NM_001042481.3:c.-147+39788_-147+39789delinsTG NP_001035946.1:n.-147+39788_-147+39789delinsTG