Canonical Allele Identifier: CA2695234057

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688395del , CM000685.2:g.48688395del	GRCh38
NC_000023.10:g.48546784del , CM000685.1:g.48546784del	GRCh37
NC_000023.9:g.48431728del	NCBI36
NG_007877.1:g.9599del , LRG_125:g.9599del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.117del
ENST00000698625.1:c.873del	ENSP00000513844.1:p.Tyr291Ter
ENST00000698626.1:c.873del	ENSP00000513845.1:p.Tyr291Ter
ENST00000698635.1:c.873del	ENSP00000513850.1:p.Tyr291Ter
ENST00000376701.5:c.873del MANE Select	ENSP00000365891.4:p.Tyr291Ter
ENST00000376701.4:c.873del	ENSP00000365891.4:p.Tyr291Ter
ENST00000474174.1:n.117del
NM_000377.2:c.873del , LRG_125t1:c.873del	NP_000368.1:p.Tyr291Ter
XM_011543977.1:c.873del	XP_011542279.1:p.Tyr291Ter
XM_011543977.2:c.873del	XP_011542279.1:p.Tyr291Ter
XM_017029786.1:c.873del	XP_016885275.1:p.Tyr291Ter
NM_000377.3:c.873del MANE Select	NP_000368.1:p.Tyr291Ter