Canonical Allele Identifier: CA2738504633

Gene: WAS

Linked Data

• dbSNP Id: rs2147265767

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688217del , CM000685.2:g.48688217del	GRCh38
NC_000023.10:g.48546606del , CM000685.1:g.48546606del	GRCh37
NC_000023.9:g.48431550del	NCBI36
NG_007877.1:g.9421del , LRG_125:g.9421del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.931del
ENST00000698625.1:c.778-83del	ENSP00000513844.1:n.778-83del
ENST00000698626.1:c.778-83del	ENSP00000513845.1:n.778-83del
ENST00000698635.1:c.778-83del	ENSP00000513850.1:n.778-83del
ENST00000376701.5:c.778-83del MANE Select	ENSP00000365891.4:n.778-83del
ENST00000376701.4:c.778-83del	ENSP00000365891.4:n.778-83del
NM_000377.2:c.778-83del , LRG_125t1:c.778-83del	NP_000368.1:n.778-83del
XM_011543977.1:c.778-83del	XP_011542279.1:n.778-83del
XM_011543977.2:c.778-83del	XP_011542279.1:n.778-83del
XM_017029786.1:c.778-83del	XP_016885275.1:n.778-83del
NM_000377.3:c.778-83del MANE Select	NP_000368.1:n.778-83del