Canonical Allele Identifier: CA2695233755

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688722del , CM000685.2:g.48688722del	GRCh38
NC_000023.10:g.48547111del , CM000685.1:g.48547111del	GRCh37
NC_000023.9:g.48432055del	NCBI36
NG_007877.1:g.9926del , LRG_125:g.9926del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.238del
ENST00000698625.1:c.994del	ENSP00000513844.1:p.Val332TrpfsTer?
ENST00000698626.1:c.994del	ENSP00000513845.1:p.Val332TrpfsTer?
ENST00000698635.1:c.994del	ENSP00000513850.1:p.Val332TrpfsTer?
ENST00000376701.5:c.994del MANE Select	ENSP00000365891.4:p.Val332TrpfsTer?
ENST00000376701.4:c.994del	ENSP00000365891.4:p.Val332TrpfsTer?
ENST00000474174.1:n.238del
NM_000377.2:c.994del , LRG_125t1:c.994del	NP_000368.1:p.Val332TrpfsTer?
XM_011543977.1:c.932-94del	XP_011542279.1:n.932-94del
XM_011543977.2:c.932-94del	XP_011542279.1:n.932-94del
XM_017029786.1:c.994del	XP_016885275.1:p.Val332TrpfsTer?
NM_000377.3:c.994del MANE Select	NP_000368.1:p.Val332TrpfsTer?