Canonical Allele Identifier: CA2693642861

Gene: WAS

Linked Data

• gnomAD v4: X-48684043-CTCCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48684046_48684049del , CM000685.2:g.48684046_48684049del	GRCh38
NC_000023.10:g.48542435_48542438del , CM000685.1:g.48542435_48542438del	GRCh37
NC_000023.9:g.48427379_48427382del	NCBI36
NG_007877.1:g.5250_5253del , LRG_125:g.5250_5253del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.165+61_165+64del
ENST00000698625.1:c.132+61_132+64del	ENSP00000513844.1:n.132+61_132+64del
ENST00000698626.1:c.132+61_132+64del	ENSP00000513845.1:n.132+61_132+64del
ENST00000698635.1:c.132+61_132+64del	ENSP00000513850.1:n.132+61_132+64del
ENST00000376701.5:c.132+61_132+64del MANE Select	ENSP00000365891.4:n.132+61_132+64del
ENST00000376701.4:c.132+61_132+64del	ENSP00000365891.4:n.132+61_132+64del
ENST00000450772.5:c.132+61_132+64del	ENSP00000410537.1:n.132+61_132+64del
ENST00000465982.5:n.167+61_167+64del
ENST00000483750.5:n.158+61_158+64del
NM_000377.2:c.132+61_132+64del , LRG_125t1:c.132+61_132+64del	NP_000368.1:n.132+61_132+64del
XM_011543977.1:c.132+61_132+64del	XP_011542279.1:n.132+61_132+64del
XM_011543977.2:c.132+61_132+64del	XP_011542279.1:n.132+61_132+64del
XM_017029786.1:c.132+61_132+64del	XP_016885275.1:n.132+61_132+64del
NM_000377.3:c.132+61_132+64del MANE Select	NP_000368.1:n.132+61_132+64del