Canonical Allele Identifier: CA2136729371

Gene: FRMD6

Linked Data

• dbSNP Id: rs1890440170

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.51610335_51610336insAA , CM000676.2:g.51610335_51610336insAA	GRCh38
NC_000014.8:g.52077053_52077054insAA , CM000676.1:g.52077053_52077054insAA	GRCh37
NC_000014.7:g.51146803_51146804insAA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356218.8:c.-147+39925_-147+39926insAA	ENSP00000348550.4:n.-147+39925_-147+39926insAA
ENST00000554745.1:n.278-33117_278-33116insAA
ENST00000556137.5:n.508+39925_508+39926insAA
NM_001042481.2:c.-147+39925_-147+39926insAA	NP_001035946.1:n.-147+39925_-147+39926insAA
XM_011536423.1:c.-147+39925_-147+39926insAA	XP_011534725.1:n.-147+39925_-147+39926insAA
XM_011536424.1:c.-147+39925_-147+39926insAA	XP_011534726.1:n.-147+39925_-147+39926insAA
XM_024449472.1:c.-147+39925_-147+39926insAA	XP_024305240.1:n.-147+39925_-147+39926insAA
XM_024449473.1:c.-146-79356_-146-79355insAA	XP_024305241.1:n.-146-79356_-146-79355insAA
NM_001042481.3:c.-147+39925_-147+39926insAA	NP_001035946.1:n.-147+39925_-147+39926insAA