Canonical Allele Identifier: CA2502436640

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48683872_48683873insT , CM000685.2:g.48683872_48683873insT	GRCh38
NC_000023.10:g.48542261_48542262insT , CM000685.1:g.48542261_48542262insT	GRCh37
NC_000023.9:g.48427205_48427206insT	NCBI36
NG_007877.1:g.5076_5077insT , LRG_125:g.5076_5077insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.52_53insT
ENST00000698625.1:c.19_20insT	ENSP00000513844.1:p.Gly7ValfsTer?
ENST00000698626.1:c.19_20insT	ENSP00000513845.1:p.Gly7ValfsTer?
ENST00000698635.1:c.19_20insT	ENSP00000513850.1:p.Gly7ValfsTer?
ENST00000376701.5:c.19_20insT MANE Select	ENSP00000365891.4:p.Gly7ValfsTer?
ENST00000376701.4:c.19_20insT	ENSP00000365891.4:p.Gly7ValfsTer?
ENST00000450772.5:c.19_20insT	ENSP00000410537.1:p.Gly7ValfsTer?
ENST00000465982.5:n.54_55insT
ENST00000483750.5:n.45_46insT
NM_000377.2:c.19_20insT , LRG_125t1:c.19_20insT	NP_000368.1:p.Gly7ValfsTer?
XM_011543977.1:c.19_20insT	XP_011542279.1:p.Gly7ValfsTer?
XM_011543977.2:c.19_20insT	XP_011542279.1:p.Gly7ValfsTer?
XM_017029786.1:c.19_20insT	XP_016885275.1:p.Gly7ValfsTer?
NM_000377.3:c.19_20insT MANE Select	NP_000368.1:p.Gly7ValfsTer?