Canonical Allele Identifier: CA2693643879

Gene: WAS

Linked Data

• gnomAD v4: X-48688003-GAGGGAAGGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688008_48688016del , CM000685.2:g.48688008_48688016del	GRCh38
NC_000023.10:g.48546397_48546405del , CM000685.1:g.48546397_48546405del	GRCh37
NC_000023.9:g.48431341_48431349del	NCBI36
NG_007877.1:g.9212_9220del , LRG_125:g.9212_9220del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.768-46_768-38del
ENST00000490627.2:n.172-46_172-38del
ENST00000698625.1:c.735-46_735-38del	ENSP00000513844.1:n.735-46_735-38del
ENST00000698626.1:c.735-46_735-38del	ENSP00000513845.1:n.735-46_735-38del
ENST00000698635.1:c.735-46_735-38del	ENSP00000513850.1:n.735-46_735-38del
ENST00000376701.5:c.735-46_735-38del MANE Select	ENSP00000365891.4:n.735-46_735-38del
ENST00000376701.4:c.735-46_735-38del	ENSP00000365891.4:n.735-46_735-38del
ENST00000465982.5:n.635-46_635-38del
ENST00000483750.5:n.761-46_761-38del
ENST00000490627.1:n.155-46_155-38del
NM_000377.2:c.735-46_735-38del , LRG_125t1:c.735-46_735-38del	NP_000368.1:n.735-46_735-38del
XM_011543977.1:c.735-46_735-38del	XP_011542279.1:n.735-46_735-38del
XM_011543977.2:c.735-46_735-38del	XP_011542279.1:n.735-46_735-38del
XM_017029786.1:c.735-46_735-38del	XP_016885275.1:n.735-46_735-38del
NM_000377.3:c.735-46_735-38del MANE Select	NP_000368.1:n.735-46_735-38del