Canonical Allele Identifier: CA1892118285
Gene: FRMD4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436703_14436709delinsCTATTTT , CM000672.2:g.14436703_14436709delinsCTATTTT GRCh38
NC_000010.10:g.14478702_14478708delinsCTATTTT , CM000672.1:g.14478702_14478708delinsCTATTTT GRCh37
NC_000010.9:g.14518708_14518714delinsCTATTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475141.2:c.-305+25359_-305+25365delinsAAAATAG ENSP00000473870.1:n.-305+25359_-305+25365delinsAAAATAG
ENST00000493380.5:c.-82+25359_-82+25365delinsAAAATAG ENSP00000474863.1:n.-82+25359_-82+25365delinsAAAATAG