Canonical Allele Identifier: CA2695234059

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688411del , CM000685.2:g.48688411del	GRCh38
NC_000023.10:g.48546800del , CM000685.1:g.48546800del	GRCh37
NC_000023.9:g.48431744del	NCBI36
NG_007877.1:g.9615del , LRG_125:g.9615del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.133del
ENST00000698625.1:c.889del	ENSP00000513844.1:p.Gln297ArgfsTer11
ENST00000698626.1:c.889del	ENSP00000513845.1:p.Gln297ArgfsTer11
ENST00000698635.1:c.889del	ENSP00000513850.1:p.Gln297ArgfsTer11
ENST00000376701.5:c.889del MANE Select	ENSP00000365891.4:p.Gln297ArgfsTer11
ENST00000376701.4:c.889del	ENSP00000365891.4:p.Gln297ArgfsTer11
ENST00000474174.1:n.133del
NM_000377.2:c.889del , LRG_125t1:c.889del	NP_000368.1:p.Gln297ArgfsTer11
XM_011543977.1:c.889del	XP_011542279.1:p.Gln297ArgfsTer11
XM_011543977.2:c.889del	XP_011542279.1:p.Gln297ArgfsTer11
XM_017029786.1:c.889del	XP_016885275.1:p.Gln297ArgfsTer11
NM_000377.3:c.889del MANE Select	NP_000368.1:p.Gln297ArgfsTer11