Canonical Allele Identifier: CA2579600684

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688164_48688165del , CM000685.2:g.48688164_48688165del	GRCh38
NC_000023.10:g.48546553_48546554del , CM000685.1:g.48546553_48546554del	GRCh37
NC_000023.9:g.48431497_48431498del	NCBI36
NG_007877.1:g.9368_9369del , LRG_125:g.9368_9369del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.878_879del
ENST00000698625.1:c.777+68_777+69del	ENSP00000513844.1:n.777+68_777+69del
ENST00000698626.1:c.777+68_777+69del	ENSP00000513845.1:n.777+68_777+69del
ENST00000698635.1:c.777+68_777+69del	ENSP00000513850.1:n.777+68_777+69del
ENST00000376701.5:c.777+68_777+69del MANE Select	ENSP00000365891.4:n.777+68_777+69del
ENST00000376701.4:c.777+68_777+69del	ENSP00000365891.4:n.777+68_777+69del
ENST00000483750.5:n.871_872del
NM_000377.2:c.777+68_777+69del , LRG_125t1:c.777+68_777+69del	NP_000368.1:n.777+68_777+69del
XM_011543977.1:c.777+68_777+69del	XP_011542279.1:n.777+68_777+69del
XM_011543977.2:c.777+68_777+69del	XP_011542279.1:n.777+68_777+69del
XM_017029786.1:c.777+68_777+69del	XP_016885275.1:n.777+68_777+69del
NM_000377.3:c.777+68_777+69del MANE Select	NP_000368.1:n.777+68_777+69del