Canonical Allele Identifier: CA1139532303

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688033_48688043del , CM000685.2:g.48688033_48688043del	GRCh38
NC_000023.10:g.48546422_48546432del , CM000685.1:g.48546422_48546432del	GRCh37
NC_000023.9:g.48431366_48431376del	NCBI36
NG_007877.1:g.9237_9247del , LRG_125:g.9237_9247del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.768-21_768-11del
ENST00000490627.2:n.172-21_172-11del
ENST00000698625.1:c.735-21_735-11del	ENSP00000513844.1:n.735-21_735-11del
ENST00000698626.1:c.735-21_735-11del	ENSP00000513845.1:n.735-21_735-11del
ENST00000698635.1:c.735-21_735-11del	ENSP00000513850.1:n.735-21_735-11del
ENST00000376701.5:c.735-21_735-11del MANE Select	ENSP00000365891.4:n.735-21_735-11del
ENST00000376701.4:c.735-21_735-11del	ENSP00000365891.4:n.735-21_735-11del
ENST00000465982.5:n.635-21_635-11del
ENST00000483750.5:n.761-21_761-11del
ENST00000490627.1:n.155-21_155-11del
NM_000377.2:c.735-21_735-11del , LRG_125t1:c.735-21_735-11del	NP_000368.1:n.735-21_735-11del
XM_011543977.1:c.735-21_735-11del	XP_011542279.1:n.735-21_735-11del
XM_011543977.2:c.735-21_735-11del	XP_011542279.1:n.735-21_735-11del
XM_017029786.1:c.735-21_735-11del	XP_016885275.1:n.735-21_735-11del
NM_000377.3:c.735-21_735-11del MANE Select	NP_000368.1:n.735-21_735-11del