Canonical Allele Identifier: CA2695233950

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48683957_48683958delinsAT , CM000685.2:g.48683957_48683958delinsAT	GRCh38
NC_000023.10:g.48542346_48542347delinsAT , CM000685.1:g.48542346_48542347delinsAT	GRCh37
NC_000023.9:g.48427290_48427291delinsAT	NCBI36
NG_007877.1:g.5161_5162delinsAT , LRG_125:g.5161_5162delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.137_138delinsAT
ENST00000698625.1:c.104_105delinsAT	ENSP00000513844.1:p.Leu35His
ENST00000698626.1:c.104_105delinsAT	ENSP00000513845.1:p.Leu35His
ENST00000698635.1:c.104_105delinsAT	ENSP00000513850.1:p.Leu35His
ENST00000376701.5:c.104_105delinsAT MANE Select	ENSP00000365891.4:p.Leu35His
ENST00000376701.4:c.104_105delinsAT	ENSP00000365891.4:p.Leu35His
ENST00000450772.5:c.104_105delinsAT	ENSP00000410537.1:p.Leu35His
ENST00000465982.5:n.139_140delinsAT
ENST00000483750.5:n.130_131delinsAT
NM_000377.2:c.104_105delinsAT , LRG_125t1:c.104_105delinsAT	NP_000368.1:p.Leu35His
XM_011543977.1:c.104_105delinsAT	XP_011542279.1:p.Leu35His
XM_011543977.2:c.104_105delinsAT	XP_011542279.1:p.Leu35His
XM_017029786.1:c.104_105delinsAT	XP_016885275.1:p.Leu35His
NM_000377.3:c.104_105delinsAT MANE Select	NP_000368.1:p.Leu35His