Canonical Allele Identifier: CA592244891
Gene: FRMD4A HGNC NCBI

Linked Data

dbSNP Id: rs1388445096
gnomAD v2: 10-14478973-ATC-A
gnomAD v3: 10-14436974-ATC-A
gnomAD v4: 10-14436974-ATC-A
MyVariant Identifiers: chr10:g.14478974_14478975del (hg19) chr10:g.14436975_14436976del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436986_14436987del , CM000672.2:g.14436986_14436987del GRCh38
NC_000010.10:g.14478985_14478986del , CM000672.1:g.14478985_14478986del GRCh37
NC_000010.9:g.14518991_14518992del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475141.2:c.-305+25092_-305+25093del ENSP00000473870.1:n.-305+25092_-305+25093del
ENST00000493380.5:c.-82+25092_-82+25093del ENSP00000474863.1:n.-82+25092_-82+25093del
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