Canonical Allele Identifier: CA592244867
Gene: FRMD4A HGNC NCBI

Linked Data

dbSNP Id: rs1388643161
gnomAD v2: 10-14478702-CTATTTT-C
gnomAD v4: 10-14436703-CTATTTT-C
MyVariant Identifiers: chr10:g.14478703_14478708del (hg19) chr10:g.14436704_14436709del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436705_14436710del , CM000672.2:g.14436705_14436710del GRCh38
NC_000010.10:g.14478704_14478709del , CM000672.1:g.14478704_14478709del GRCh37
NC_000010.9:g.14518710_14518715del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475141.2:c.-305+25359_-305+25364del ENSP00000473870.1:n.-305+25359_-305+25364del
ENST00000493380.5:c.-82+25359_-82+25364del ENSP00000474863.1:n.-82+25359_-82+25364del
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