Canonical Allele Identifier: CA2693644674

Gene: WAS

Linked Data

• gnomAD v4: X-48688807-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688808del , CM000685.2:g.48688808del	GRCh38
NC_000023.10:g.48547197del , CM000685.1:g.48547197del	GRCh37
NC_000023.9:g.48432141del	NCBI36
NG_007877.1:g.10012del , LRG_125:g.10012del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.324del
ENST00000698625.1:c.1080del	ENSP00000513844.1:p.Pro362GlnfsTer?
ENST00000698626.1:c.1080del	ENSP00000513845.1:p.Pro362GlnfsTer?
ENST00000698635.1:c.1080del	ENSP00000513850.1:p.Pro362GlnfsTer?
ENST00000376701.5:c.1080del MANE Select	ENSP00000365891.4:p.Pro362GlnfsTer?
ENST00000376701.4:c.1080del	ENSP00000365891.4:p.Pro362GlnfsTer?
ENST00000474174.1:n.324del
NM_000377.2:c.1080del , LRG_125t1:c.1080del	NP_000368.1:p.Pro362GlnfsTer?
XM_011543977.1:c.932-8del	XP_011542279.1:n.932-8del
XM_011543977.2:c.932-8del	XP_011542279.1:n.932-8del
XM_017029786.1:c.1080del	XP_016885275.1:p.Pro362GlnfsTer?
NM_000377.3:c.1080del MANE Select	NP_000368.1:p.Pro362GlnfsTer?