Canonical Allele Identifier: CA2428354237

Gene: WAS

Linked Data

• dbSNP Id: rs2062411352

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48684048_48684050del , CM000685.2:g.48684048_48684050del	GRCh38
NC_000023.10:g.48542437_48542439del , CM000685.1:g.48542437_48542439del	GRCh37
NC_000023.9:g.48427381_48427383del	NCBI36
NG_007877.1:g.5252_5254del , LRG_125:g.5252_5254del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.165+63_165+65del
ENST00000698625.1:c.132+63_132+65del	ENSP00000513844.1:n.132+63_132+65del
ENST00000698626.1:c.132+63_132+65del	ENSP00000513845.1:n.132+63_132+65del
ENST00000698635.1:c.132+63_132+65del	ENSP00000513850.1:n.132+63_132+65del
ENST00000376701.5:c.132+63_132+65del MANE Select	ENSP00000365891.4:n.132+63_132+65del
ENST00000376701.4:c.132+63_132+65del	ENSP00000365891.4:n.132+63_132+65del
ENST00000450772.5:c.132+63_132+65del	ENSP00000410537.1:n.132+63_132+65del
ENST00000465982.5:n.167+63_167+65del
ENST00000483750.5:n.158+63_158+65del
NM_000377.2:c.132+63_132+65del , LRG_125t1:c.132+63_132+65del	NP_000368.1:n.132+63_132+65del
XM_011543977.1:c.132+63_132+65del	XP_011542279.1:n.132+63_132+65del
XM_011543977.2:c.132+63_132+65del	XP_011542279.1:n.132+63_132+65del
XM_017029786.1:c.132+63_132+65del	XP_016885275.1:n.132+63_132+65del
NM_000377.3:c.132+63_132+65del MANE Select	NP_000368.1:n.132+63_132+65del