Canonical Allele Identifier: CA2428355669

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688778C= , CM000685.2:g.48688778C=	GRCh38
NC_000023.10:g.48547167C= , CM000685.1:g.48547167C=	GRCh37
NC_000023.9:g.48432111C=	NCBI36
NG_007877.1:g.9982C= , LRG_125:g.9982C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.294C=
ENST00000698625.1:c.1050C=	ENSP00000513844.1:p.Ala350=
ENST00000698626.1:c.1050C=	ENSP00000513845.1:p.Ala350=
ENST00000698635.1:c.1050C=	ENSP00000513850.1:p.Ala350=
ENST00000376701.5:c.1050C= MANE Select	ENSP00000365891.4:p.Ala350=
ENST00000376701.4:c.1050C=	ENSP00000365891.4:p.Ala350=
ENST00000474174.1:n.294C=
NM_000377.2:c.1050C= , LRG_125t1:c.1050C=	NP_000368.1:p.Ala350=
XM_011543977.1:c.932-38C=	XP_011542279.1:n.932-38C=
XM_011543977.2:c.932-38C=	XP_011542279.1:n.932-38C=
XM_017029786.1:c.1050C=	XP_016885275.1:p.Ala350=
NM_000377.3:c.1050C= MANE Select	NP_000368.1:p.Ala350=