Canonical Allele Identifier: CA2693643952

Gene: WAS

Linked Data

• gnomAD v4: X-48688123-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688125del , CM000685.2:g.48688125del	GRCh38
NC_000023.10:g.48546514del , CM000685.1:g.48546514del	GRCh37
NC_000023.9:g.48431458del	NCBI36
NG_007877.1:g.9329del , LRG_125:g.9329del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.839del
ENST00000490627.2:n.243del
ENST00000698625.1:c.777+29del	ENSP00000513844.1:n.777+29del
ENST00000698626.1:c.777+29del	ENSP00000513845.1:n.777+29del
ENST00000698635.1:c.777+29del	ENSP00000513850.1:n.777+29del
ENST00000376701.5:c.777+29del MANE Select	ENSP00000365891.4:n.777+29del
ENST00000376701.4:c.777+29del	ENSP00000365891.4:n.777+29del
ENST00000465982.5:n.706del
ENST00000483750.5:n.832del
ENST00000490627.1:n.226del
NM_000377.2:c.777+29del , LRG_125t1:c.777+29del	NP_000368.1:n.777+29del
XM_011543977.1:c.777+29del	XP_011542279.1:n.777+29del
XM_011543977.2:c.777+29del	XP_011542279.1:n.777+29del
XM_017029786.1:c.777+29del	XP_016885275.1:n.777+29del
NM_000377.3:c.777+29del MANE Select	NP_000368.1:n.777+29del