Canonical Allele Identifier: CA2693643866

Gene: WAS

Linked Data

• gnomAD v4: X-48687964-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48687966_48687967del , CM000685.2:g.48687966_48687967del	GRCh38
NC_000023.10:g.48546355_48546356del , CM000685.1:g.48546355_48546356del	GRCh37
NC_000023.9:g.48431299_48431300del	NCBI36
NG_007877.1:g.9170_9171del , LRG_125:g.9170_9171del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.768-88_768-87del
ENST00000490627.2:n.172-88_172-87del
ENST00000698625.1:c.735-88_735-87del	ENSP00000513844.1:n.735-88_735-87del
ENST00000698626.1:c.735-88_735-87del	ENSP00000513845.1:n.735-88_735-87del
ENST00000698635.1:c.735-88_735-87del	ENSP00000513850.1:n.735-88_735-87del
ENST00000376701.5:c.735-88_735-87del MANE Select	ENSP00000365891.4:n.735-88_735-87del
ENST00000376701.4:c.735-88_735-87del	ENSP00000365891.4:n.735-88_735-87del
ENST00000465982.5:n.635-88_635-87del
ENST00000483750.5:n.761-88_761-87del
ENST00000490627.1:n.155-88_155-87del
NM_000377.2:c.735-88_735-87del , LRG_125t1:c.735-88_735-87del	NP_000368.1:n.735-88_735-87del
XM_011543977.1:c.735-88_735-87del	XP_011542279.1:n.735-88_735-87del
XM_011543977.2:c.735-88_735-87del	XP_011542279.1:n.735-88_735-87del
XM_017029786.1:c.735-88_735-87del	XP_016885275.1:n.735-88_735-87del
NM_000377.3:c.735-88_735-87del MANE Select	NP_000368.1:n.735-88_735-87del