Canonical Allele Identifier: CA2428355461

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688075G= , CM000685.2:g.48688075G=	GRCh38
NC_000023.10:g.48546464G= , CM000685.1:g.48546464G=	GRCh37
NC_000023.9:g.48431408G=	NCBI36
NG_007877.1:g.9279G= , LRG_125:g.9279G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.789G=
ENST00000490627.2:n.193G=
ENST00000698625.1:c.756G=	ENSP00000513844.1:p.Trp252=
ENST00000698626.1:c.756G=	ENSP00000513845.1:p.Trp252=
ENST00000698635.1:c.756G=	ENSP00000513850.1:p.Trp252=
ENST00000376701.5:c.756G= MANE Select	ENSP00000365891.4:p.Trp252=
ENST00000376701.4:c.756G=	ENSP00000365891.4:p.Trp252=
ENST00000465982.5:n.656G=
ENST00000483750.5:n.782G=
ENST00000490627.1:n.176G=
NM_000377.2:c.756G= , LRG_125t1:c.756G=	NP_000368.1:p.Trp252=
XM_011543977.1:c.756G=	XP_011542279.1:p.Trp252=
XM_011543977.2:c.756G=	XP_011542279.1:p.Trp252=
XM_017029786.1:c.756G=	XP_016885275.1:p.Trp252=
NM_000377.3:c.756G= MANE Select	NP_000368.1:p.Trp252=