Canonical Allele Identifier: CA2693643860

Gene: WAS

Linked Data

• gnomAD v4: X-48687956-CAGAGTCTCTTTGGGCAGGAGAGGGCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48687961_48687986del , CM000685.2:g.48687961_48687986del	GRCh38
NC_000023.10:g.48546350_48546375del , CM000685.1:g.48546350_48546375del	GRCh37
NC_000023.9:g.48431294_48431319del	NCBI36
NG_007877.1:g.9165_9190del , LRG_125:g.9165_9190del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.768-93_768-68del
ENST00000490627.2:n.172-93_172-68del
ENST00000698625.1:c.735-93_735-68del	ENSP00000513844.1:n.735-93_735-68del
ENST00000698626.1:c.735-93_735-68del	ENSP00000513845.1:n.735-93_735-68del
ENST00000698635.1:c.735-93_735-68del	ENSP00000513850.1:n.735-93_735-68del
ENST00000376701.5:c.735-93_735-68del MANE Select	ENSP00000365891.4:n.735-93_735-68del
ENST00000376701.4:c.735-93_735-68del	ENSP00000365891.4:n.735-93_735-68del
ENST00000465982.5:n.635-93_635-68del
ENST00000483750.5:n.761-93_761-68del
ENST00000490627.1:n.155-93_155-68del
NM_000377.2:c.735-93_735-68del , LRG_125t1:c.735-93_735-68del	NP_000368.1:n.735-93_735-68del
XM_011543977.1:c.735-93_735-68del	XP_011542279.1:n.735-93_735-68del
XM_011543977.2:c.735-93_735-68del	XP_011542279.1:n.735-93_735-68del
XM_017029786.1:c.735-93_735-68del	XP_016885275.1:n.735-93_735-68del
NM_000377.3:c.735-93_735-68del MANE Select	NP_000368.1:n.735-93_735-68del