Canonical Allele Identifier: CA2428355658

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688727G= , CM000685.2:g.48688727G=	GRCh38
NC_000023.10:g.48547116G= , CM000685.1:g.48547116G=	GRCh37
NC_000023.9:g.48432060G=	NCBI36
NG_007877.1:g.9931G= , LRG_125:g.9931G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.243G=
ENST00000698625.1:c.999G=	ENSP00000513844.1:p.Gly333=
ENST00000698626.1:c.999G=	ENSP00000513845.1:p.Gly333=
ENST00000698635.1:c.999G=	ENSP00000513850.1:p.Gly333=
ENST00000376701.5:c.999G= MANE Select	ENSP00000365891.4:p.Gly333=
ENST00000376701.4:c.999G=	ENSP00000365891.4:p.Gly333=
ENST00000474174.1:n.243G=
NM_000377.2:c.999G= , LRG_125t1:c.999G=	NP_000368.1:p.Gly333=
XM_011543977.1:c.932-89G=	XP_011542279.1:n.932-89G=
XM_011543977.2:c.932-89G=	XP_011542279.1:n.932-89G=
XM_017029786.1:c.999G=	XP_016885275.1:p.Gly333=
NM_000377.3:c.999G= MANE Select	NP_000368.1:p.Gly333=