Canonical Allele Identifier: CA2840872481

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48687983dup , CM000685.2:g.48687983dup	GRCh38
NC_000023.10:g.48546372dup , CM000685.1:g.48546372dup	GRCh37
NC_000023.9:g.48431316dup	NCBI36
NG_007877.1:g.9187dup , LRG_125:g.9187dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.768-71dup
ENST00000490627.2:n.172-71dup
ENST00000698625.1:c.735-71dup	ENSP00000513844.1:n.735-71dup
ENST00000698626.1:c.735-71dup	ENSP00000513845.1:n.735-71dup
ENST00000698635.1:c.735-71dup	ENSP00000513850.1:n.735-71dup
ENST00000376701.5:c.735-71dup MANE Select	ENSP00000365891.4:n.735-71dup
ENST00000376701.4:c.735-71dup	ENSP00000365891.4:n.735-71dup
ENST00000465982.5:n.635-71dup
ENST00000483750.5:n.761-71dup
ENST00000490627.1:n.155-71dup
NM_000377.2:c.735-71dup , LRG_125t1:c.735-71dup	NP_000368.1:n.735-71dup
XM_011543977.1:c.735-71dup	XP_011542279.1:n.735-71dup
XM_011543977.2:c.735-71dup	XP_011542279.1:n.735-71dup
XM_017029786.1:c.735-71dup	XP_016885275.1:n.735-71dup
NM_000377.3:c.735-71dup MANE Select	NP_000368.1:n.735-71dup