Canonical Allele Identifier: CA329099824

Gene: WAS

Linked Data

• dbSNP Id: rs781985914
• gnomAD v3: X-48683755-G-GT
• gnomAD v4: X-48683755-G-GT
• MyVariant Identifiers: chrX:g.48542144_48542145insT (hg19) ; chrX:g.48683755_48683756insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48683761dup , CM000685.2:g.48683761dup	GRCh38
NC_000023.10:g.48542150dup , CM000685.1:g.48542150dup	GRCh37
NC_000023.9:g.48427094dup	NCBI36
NG_007877.1:g.4965dup , LRG_125:g.4965dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698625.1:c.-34-59dup	ENSP00000513844.1:n.-34-59dup
ENST00000450772.5:c.-34-59dup	ENSP00000410537.1:n.-34-59dup
XM_017029786.1:c.-93dup	XP_016885275.1:n.-93dup