Canonical Allele Identifier: CA2693644698

Gene: WAS

Linked Data

• gnomAD v4: X-48688813-CAGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688814_48688816del , CM000685.2:g.48688814_48688816del	GRCh38
NC_000023.10:g.48547203_48547205del , CM000685.1:g.48547203_48547205del	GRCh37
NC_000023.9:g.48432147_48432149del	NCBI36
NG_007877.1:g.10018_10020del , LRG_125:g.10018_10020del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.330_332del
ENST00000698625.1:c.1086_1088del	ENSP00000513844.1:p.Gly363del
ENST00000698626.1:c.1086_1088del	ENSP00000513845.1:p.Gly363del
ENST00000698635.1:c.1086_1088del	ENSP00000513850.1:p.Gly363del
ENST00000376701.5:c.1086_1088del MANE Select	ENSP00000365891.4:p.Gly363del
ENST00000376701.4:c.1086_1088del	ENSP00000365891.4:p.Gly363del
ENST00000474174.1:n.330_332del
NM_000377.2:c.1086_1088del , LRG_125t1:c.1086_1088del	NP_000368.1:p.Gly363del
XM_011543977.1:c.932-2_932del
XM_011543977.2:c.932-2_932del
XM_017029786.1:c.1086_1088del	XP_016885275.1:p.Gly363del
NM_000377.3:c.1086_1088del MANE Select	NP_000368.1:p.Gly363del