Canonical Allele Identifier: CA2551081065

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48683851del , CM000685.2:g.48683851del	GRCh38
NC_000023.10:g.48542240del , CM000685.1:g.48542240del	GRCh37
NC_000023.9:g.48427184del	NCBI36
NG_007877.1:g.5055del , LRG_125:g.5055del

Transcript Alleles

HGVS	Amino-acid change
ENST00000483750.6:n.31del
ENST00000698625.1:c.-3del	ENSP00000513844.1:n.-3del
ENST00000698626.1:c.-3del	ENSP00000513845.1:n.-3del
ENST00000698635.1:c.-3del	ENSP00000513850.1:n.-3del
ENST00000376701.5:c.-3del MANE Select	ENSP00000365891.4:n.-3del
ENST00000376701.4:c.-3del	ENSP00000365891.4:n.-3del
ENST00000450772.5:c.-3del	ENSP00000410537.1:n.-3del
ENST00000465982.5:n.33del
ENST00000483750.5:n.24del
NM_000377.2:c.-3del , LRG_125t1:c.-3del	NP_000368.1:n.-3del
XM_011543977.1:c.-3del	XP_011542279.1:n.-3del
XM_011543977.2:c.-3del	XP_011542279.1:n.-3del
XM_017029786.1:c.-3del	XP_016885275.1:n.-3del
NM_000377.3:c.-3del MANE Select	NP_000368.1:n.-3del