Canonical Allele Identifier: CA2693643831

Gene: WAS

Linked Data

• gnomAD v4: X-48687913-TACTCATTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48687923_48687930del , CM000685.2:g.48687923_48687930del	GRCh38
NC_000023.10:g.48546312_48546319del , CM000685.1:g.48546312_48546319del	GRCh37
NC_000023.9:g.48431256_48431263del	NCBI36
NG_007877.1:g.9127_9134del , LRG_125:g.9127_9134del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.768-131_768-124del
ENST00000490627.2:n.172-131_172-124del
ENST00000698625.1:c.735-131_735-124del	ENSP00000513844.1:n.735-131_735-124del
ENST00000698626.1:c.735-131_735-124del	ENSP00000513845.1:n.735-131_735-124del
ENST00000698635.1:c.735-131_735-124del	ENSP00000513850.1:n.735-131_735-124del
ENST00000376701.5:c.735-131_735-124del MANE Select	ENSP00000365891.4:n.735-131_735-124del
ENST00000376701.4:c.735-131_735-124del	ENSP00000365891.4:n.735-131_735-124del
ENST00000465982.5:n.635-131_635-124del
ENST00000483750.5:n.761-131_761-124del
ENST00000490627.1:n.155-131_155-124del
NM_000377.2:c.735-131_735-124del , LRG_125t1:c.735-131_735-124del	NP_000368.1:n.735-131_735-124del
XM_011543977.1:c.735-131_735-124del	XP_011542279.1:n.735-131_735-124del
XM_011543977.2:c.735-131_735-124del	XP_011542279.1:n.735-131_735-124del
XM_017029786.1:c.735-131_735-124del	XP_016885275.1:n.735-131_735-124del
NM_000377.3:c.735-131_735-124del MANE Select	NP_000368.1:n.735-131_735-124del