Canonical Allele Identifier: CA2695233973

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48685551_48685552del , CM000685.2:g.48685551_48685552del	GRCh38
NC_000023.10:g.48543940_48543941del , CM000685.1:g.48543940_48543941del	GRCh37
NC_000023.9:g.48428884_48428885del	NCBI36
NG_007877.1:g.6755_6756del , LRG_125:g.6755_6756del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.311_312del
ENST00000698625.1:c.278_279del	ENSP00000513844.1:p.Gly93AlafsTer28
ENST00000698626.1:c.278_279del	ENSP00000513845.1:p.Gly93AlafsTer28
ENST00000698635.1:c.278_279del	ENSP00000513850.1:p.Gly93AlafsTer28
ENST00000376701.5:c.278_279del MANE Select	ENSP00000365891.4:p.Gly93AlafsTer28
ENST00000376701.4:c.278_279del	ENSP00000365891.4:p.Gly93AlafsTer28
ENST00000450772.5:c.278_279del	ENSP00000410537.1:p.Gly93AlafsTer28
ENST00000465982.5:n.313_314del
ENST00000483750.5:n.304_305del
NM_000377.2:c.278_279del , LRG_125t1:c.278_279del	NP_000368.1:p.Gly93AlafsTer28
XM_011543977.1:c.278_279del	XP_011542279.1:p.Gly93AlafsTer28
XM_011543977.2:c.278_279del	XP_011542279.1:p.Gly93AlafsTer28
XM_017029786.1:c.278_279del	XP_016885275.1:p.Gly93AlafsTer28
NM_000377.3:c.278_279del MANE Select	NP_000368.1:p.Gly93AlafsTer28