Canonical Allele Identifier: CA2579600696

Gene: WAS

Linked Data

• gnomAD v4: X-48688278-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688280dup , CM000685.2:g.48688280dup	GRCh38
NC_000023.10:g.48546669dup , CM000685.1:g.48546669dup	GRCh37
NC_000023.9:g.48431613dup	NCBI36
NG_007877.1:g.9484dup , LRG_125:g.9484dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.2dup
ENST00000483750.6:n.994dup
ENST00000698625.1:c.778-20dup	ENSP00000513844.1:n.778-20dup
ENST00000698626.1:c.778-20dup	ENSP00000513845.1:n.778-20dup
ENST00000698635.1:c.778-20dup	ENSP00000513850.1:n.778-20dup
ENST00000376701.5:c.778-20dup MANE Select	ENSP00000365891.4:n.778-20dup
ENST00000376701.4:c.778-20dup	ENSP00000365891.4:n.778-20dup
ENST00000474174.1:n.2dup
NM_000377.2:c.778-20dup , LRG_125t1:c.778-20dup	NP_000368.1:n.778-20dup
XM_011543977.1:c.778-20dup	XP_011542279.1:n.778-20dup
XM_011543977.2:c.778-20dup	XP_011542279.1:n.778-20dup
XM_017029786.1:c.778-20dup	XP_016885275.1:n.778-20dup
NM_000377.3:c.778-20dup MANE Select	NP_000368.1:n.778-20dup