Canonical Allele Identifier: CA1892118196
Gene: FRMD4A HGNC NCBI
MIR1265 HGNC NCBI

Linked Data

dbSNP Id: rs1844559589

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436602del , CM000672.2:g.14436602del GRCh38
NC_000010.10:g.14478601del , CM000672.1:g.14478601del GRCh37
NC_000010.9:g.14518607del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475141.2:c.-305+25467del (FRMD4A) ENSP00000473870.1:n.-305+25467del
ENST00000493380.5:c.-82+25467del (FRMD4A) ENSP00000474863.1:n.-82+25467del
NR_031668.1:n.27del (MIR1265)