Canonical Allele Identifier: CA2428355466

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688108_48688110delinsCAG , CM000685.2:g.48688108_48688110delinsCAG	GRCh38
NC_000023.10:g.48546497_48546499delinsCAG , CM000685.1:g.48546497_48546499delinsCAG	GRCh37
NC_000023.9:g.48431441_48431443delinsCAG	NCBI36
NG_007877.1:g.9312_9314delinsCAG , LRG_125:g.9312_9314delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.822_824delinsCAG
ENST00000490627.2:n.226_228delinsCAG
ENST00000698625.1:c.777+12_777+14delinsCAG	ENSP00000513844.1:n.777+12_777+14delinsCAG
ENST00000698626.1:c.777+12_777+14delinsCAG	ENSP00000513845.1:n.777+12_777+14delinsCAG
ENST00000698635.1:c.777+12_777+14delinsCAG	ENSP00000513850.1:n.777+12_777+14delinsCAG
ENST00000376701.5:c.777+12_777+14delinsCAG MANE Select	ENSP00000365891.4:n.777+12_777+14delinsCAG
ENST00000376701.4:c.777+12_777+14delinsCAG	ENSP00000365891.4:n.777+12_777+14delinsCAG
ENST00000465982.5:n.689_691delinsCAG
ENST00000483750.5:n.815_817delinsCAG
ENST00000490627.1:n.209_211delinsCAG
NM_000377.2:c.777+12_777+14delinsCAG , LRG_125t1:c.777+12_777+14delinsCAG	NP_000368.1:n.777+12_777+14delinsCAG
XM_011543977.1:c.777+12_777+14delinsCAG	XP_011542279.1:n.777+12_777+14delinsCAG
XM_011543977.2:c.777+12_777+14delinsCAG	XP_011542279.1:n.777+12_777+14delinsCAG
XM_017029786.1:c.777+12_777+14delinsCAG	XP_016885275.1:n.777+12_777+14delinsCAG
NM_000377.3:c.777+12_777+14delinsCAG MANE Select	NP_000368.1:n.777+12_777+14delinsCAG