Canonical Allele Identifier: CA1892118226
Gene: FRMD4A HGNC NCBI
MIR1265 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436630T= , CM000672.2:g.14436630T= GRCh38
NC_000010.10:g.14478629T= , CM000672.1:g.14478629T= GRCh37
NC_000010.9:g.14518635T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475141.2:c.-305+25438A= (FRMD4A) ENSP00000473870.1:n.-305+25438A=
ENST00000493380.5:c.-82+25438A= (FRMD4A) ENSP00000474863.1:n.-82+25438A=
NR_031668.1:n.55T= (MIR1265)