Canonical Allele Identifier: CA2428355516

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688282_48688283delinsCT , CM000685.2:g.48688282_48688283delinsCT	GRCh38
NC_000023.10:g.48546671_48546672delinsCT , CM000685.1:g.48546671_48546672delinsCT	GRCh37
NC_000023.9:g.48431615_48431616delinsCT	NCBI36
NG_007877.1:g.9486_9487delinsCT , LRG_125:g.9486_9487delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.4_5delinsCT
ENST00000483750.6:n.996_997delinsCT
ENST00000698625.1:c.778-18_778-17delinsCT	ENSP00000513844.1:n.778-18_778-17delinsCT
ENST00000698626.1:c.778-18_778-17delinsCT	ENSP00000513845.1:n.778-18_778-17delinsCT
ENST00000698635.1:c.778-18_778-17delinsCT	ENSP00000513850.1:n.778-18_778-17delinsCT
ENST00000376701.5:c.778-18_778-17delinsCT MANE Select	ENSP00000365891.4:n.778-18_778-17delinsCT
ENST00000376701.4:c.778-18_778-17delinsCT	ENSP00000365891.4:n.778-18_778-17delinsCT
ENST00000474174.1:n.4_5delinsCT
NM_000377.2:c.778-18_778-17delinsCT , LRG_125t1:c.778-18_778-17delinsCT	NP_000368.1:n.778-18_778-17delinsCT
XM_011543977.1:c.778-18_778-17delinsCT	XP_011542279.1:n.778-18_778-17delinsCT
XM_011543977.2:c.778-18_778-17delinsCT	XP_011542279.1:n.778-18_778-17delinsCT
XM_017029786.1:c.778-18_778-17delinsCT	XP_016885275.1:n.778-18_778-17delinsCT
NM_000377.3:c.778-18_778-17delinsCT MANE Select	NP_000368.1:n.778-18_778-17delinsCT