Canonical Allele Identifier: CA2428355457

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688057T= , CM000685.2:g.48688057T=	GRCh38
NC_000023.10:g.48546446T= , CM000685.1:g.48546446T=	GRCh37
NC_000023.9:g.48431390T=	NCBI36
NG_007877.1:g.9261T= , LRG_125:g.9261T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.771T=
ENST00000490627.2:n.175T=
ENST00000698625.1:c.738T=	ENSP00000513844.1:p.His246=
ENST00000698626.1:c.738T=	ENSP00000513845.1:p.His246=
ENST00000698635.1:c.738T=	ENSP00000513850.1:p.His246=
ENST00000376701.5:c.738T= MANE Select	ENSP00000365891.4:p.His246=
ENST00000376701.4:c.738T=	ENSP00000365891.4:p.His246=
ENST00000465982.5:n.638T=
ENST00000483750.5:n.764T=
ENST00000490627.1:n.158T=
NM_000377.2:c.738T= , LRG_125t1:c.738T=	NP_000368.1:p.His246=
XM_011543977.1:c.738T=	XP_011542279.1:p.His246=
XM_011543977.2:c.738T=	XP_011542279.1:p.His246=
XM_017029786.1:c.738T=	XP_016885275.1:p.His246=
NM_000377.3:c.738T= MANE Select	NP_000368.1:p.His246=