Canonical Allele Identifier: CA2695234046

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688098_48688099del , CM000685.2:g.48688098_48688099del	GRCh38
NC_000023.10:g.48546487_48546488del , CM000685.1:g.48546487_48546488del	GRCh37
NC_000023.9:g.48431431_48431432del	NCBI36
NG_007877.1:g.9302_9303del , LRG_125:g.9302_9303del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.812_813del
ENST00000490627.2:n.216_217del
ENST00000698625.1:c.777+2_777+3del	ENSP00000513844.1:n.777+2_777+3del
ENST00000698626.1:c.777+2_777+3del	ENSP00000513845.1:n.777+2_777+3del
ENST00000698635.1:c.777+2_777+3del	ENSP00000513850.1:n.777+2_777+3del
ENST00000376701.5:c.777+2_777+3del MANE Select	ENSP00000365891.4:n.777+2_777+3del
ENST00000376701.4:c.777+2_777+3del	ENSP00000365891.4:n.777+2_777+3del
ENST00000465982.5:n.679_680del
ENST00000483750.5:n.805_806del
ENST00000490627.1:n.199_200del
NM_000377.2:c.777+2_777+3del , LRG_125t1:c.777+2_777+3del	NP_000368.1:n.777+2_777+3del
XM_011543977.1:c.777+2_777+3del	XP_011542279.1:n.777+2_777+3del
XM_011543977.2:c.777+2_777+3del	XP_011542279.1:n.777+2_777+3del
XM_017029786.1:c.777+2_777+3del	XP_016885275.1:n.777+2_777+3del
NM_000377.3:c.777+2_777+3del MANE Select	NP_000368.1:n.777+2_777+3del