Canonical Allele Identifier: CA2695233789

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688948_48688949dup , CM000685.2:g.48688948_48688949dup	GRCh38
NC_000023.10:g.48547337_48547338dup , CM000685.1:g.48547337_48547338dup	GRCh37
NC_000023.9:g.48432281_48432282dup	NCBI36
NG_007877.1:g.10152_10153dup , LRG_125:g.10152_10153dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.464_465dup
ENST00000698625.1:c.1220_1221dup	ENSP00000513844.1:p.Asn408GlyfsTer?
ENST00000698626.1:c.1220_1221dup	ENSP00000513845.1:p.Asn408GlyfsTer?
ENST00000698635.1:c.1220_1221dup	ENSP00000513850.1:p.Asn408GlyfsTer?
ENST00000376701.5:c.1220_1221dup MANE Select	ENSP00000365891.4:p.Asn408GlyfsTer?
ENST00000376701.4:c.1220_1221dup	ENSP00000365891.4:p.Asn408GlyfsTer?
ENST00000474174.1:n.464_465dup
NM_000377.2:c.1220_1221dup , LRG_125t1:c.1220_1221dup	NP_000368.1:p.Asn408GlyfsTer?
XM_011543977.1:c.1064_1065dup	XP_011542279.1:p.Asn356GlyfsTer?
XM_011543977.2:c.1064_1065dup	XP_011542279.1:p.Asn356GlyfsTer?
XM_017029786.1:c.1220_1221dup	XP_016885275.1:p.Asn408GlyfsTer?
NM_000377.3:c.1220_1221dup MANE Select	NP_000368.1:p.Asn408GlyfsTer?