Canonical Allele Identifier: CA2579600571

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48684060_48684061insG , CM000685.2:g.48684060_48684061insG	GRCh38
NC_000023.10:g.48542449_48542450insG , CM000685.1:g.48542449_48542450insG	GRCh37
NC_000023.9:g.48427393_48427394insG	NCBI36
NG_007877.1:g.5264_5265insG , LRG_125:g.5264_5265insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.165+75_165+76insG
ENST00000698625.1:c.132+75_132+76insG	ENSP00000513844.1:n.132+75_132+76insG
ENST00000698626.1:c.132+75_132+76insG	ENSP00000513845.1:n.132+75_132+76insG
ENST00000698635.1:c.132+75_132+76insG	ENSP00000513850.1:n.132+75_132+76insG
ENST00000376701.5:c.132+75_132+76insG MANE Select	ENSP00000365891.4:n.132+75_132+76insG
ENST00000376701.4:c.132+75_132+76insG	ENSP00000365891.4:n.132+75_132+76insG
ENST00000450772.5:c.132+75_132+76insG	ENSP00000410537.1:n.132+75_132+76insG
ENST00000465982.5:n.167+75_167+76insG
ENST00000483750.5:n.158+75_158+76insG
NM_000377.2:c.132+75_132+76insG , LRG_125t1:c.132+75_132+76insG	NP_000368.1:n.132+75_132+76insG
XM_011543977.1:c.132+75_132+76insG	XP_011542279.1:n.132+75_132+76insG
XM_011543977.2:c.132+75_132+76insG	XP_011542279.1:n.132+75_132+76insG
XM_017029786.1:c.132+75_132+76insG	XP_016885275.1:n.132+75_132+76insG
NM_000377.3:c.132+75_132+76insG MANE Select	NP_000368.1:n.132+75_132+76insG