Canonical Allele Identifier: CA2428355547

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688378_48688379delinsAC , CM000685.2:g.48688378_48688379delinsAC	GRCh38
NC_000023.10:g.48546767_48546768delinsAC , CM000685.1:g.48546767_48546768delinsAC	GRCh37
NC_000023.9:g.48431711_48431712delinsAC	NCBI36
NG_007877.1:g.9582_9583delinsAC , LRG_125:g.9582_9583delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.100_101delinsAC
ENST00000483750.6:n.1092_1093delinsAC
ENST00000698625.1:c.856_857delinsAC	ENSP00000513844.1:p.Thr286=
ENST00000698626.1:c.856_857delinsAC	ENSP00000513845.1:p.Thr286=
ENST00000698635.1:c.856_857delinsAC	ENSP00000513850.1:p.Thr286=
ENST00000376701.5:c.856_857delinsAC MANE Select	ENSP00000365891.4:p.Thr286=
ENST00000376701.4:c.856_857delinsAC	ENSP00000365891.4:p.Thr286=
ENST00000474174.1:n.100_101delinsAC
NM_000377.2:c.856_857delinsAC , LRG_125t1:c.856_857delinsAC	NP_000368.1:p.Thr286=
XM_011543977.1:c.856_857delinsAC	XP_011542279.1:p.Thr286=
XM_011543977.2:c.856_857delinsAC	XP_011542279.1:p.Thr286=
XM_017029786.1:c.856_857delinsAC	XP_016885275.1:p.Thr286=
NM_000377.3:c.856_857delinsAC MANE Select	NP_000368.1:p.Thr286=