Canonical Allele Identifier: CA2695233766

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688765del , CM000685.2:g.48688765del	GRCh38
NC_000023.10:g.48547154del , CM000685.1:g.48547154del	GRCh37
NC_000023.9:g.48432098del	NCBI36
NG_007877.1:g.9969del , LRG_125:g.9969del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.281del
ENST00000698625.1:c.1037del	ENSP00000513844.1:p.Pro346LeufsTer?
ENST00000698626.1:c.1037del	ENSP00000513845.1:p.Pro346LeufsTer?
ENST00000698635.1:c.1037del	ENSP00000513850.1:p.Pro346LeufsTer?
ENST00000376701.5:c.1037del MANE Select	ENSP00000365891.4:p.Pro346LeufsTer?
ENST00000376701.4:c.1037del	ENSP00000365891.4:p.Pro346LeufsTer?
ENST00000474174.1:n.281del
NM_000377.2:c.1037del , LRG_125t1:c.1037del	NP_000368.1:p.Pro346LeufsTer?
XM_011543977.1:c.932-51del	XP_011542279.1:n.932-51del
XM_011543977.2:c.932-51del	XP_011542279.1:n.932-51del
XM_017029786.1:c.1037del	XP_016885275.1:p.Pro346LeufsTer?
NM_000377.3:c.1037del MANE Select	NP_000368.1:p.Pro346LeufsTer?