Canonical Allele Identifier: CA662079062

Gene: FRMD4A

Linked Data

• dbSNP Id: rs1472768650
• MyVariant Identifiers: chr10:g.14478712_14478713insT (hg19) ; chr10:g.14436713_14436714insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14436715dup , CM000672.2:g.14436715dup	GRCh38
NC_000010.10:g.14478714dup , CM000672.1:g.14478714dup	GRCh37
NC_000010.9:g.14518720dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475141.2:c.-305+25354dup	ENSP00000473870.1:n.-305+25354dup
ENST00000493380.5:c.-82+25354dup	ENSP00000474863.1:n.-82+25354dup