Canonical Allele Identifier: CA2428355872

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48689201T= , CM000685.2:g.48689201T=	GRCh38
NC_000023.10:g.48547590T= , CM000685.1:g.48547590T=	GRCh37
NC_000023.9:g.48432534T=	NCBI36
NG_007877.1:g.10405T= , LRG_125:g.10405T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.583-119T=
ENST00000698625.1:c.1339-119T=	ENSP00000513844.1:n.1339-119T=
ENST00000698626.1:c.1339-119T=	ENSP00000513845.1:n.1339-119T=
ENST00000698635.1:c.1339-119T=	ENSP00000513850.1:n.1339-119T=
ENST00000376701.5:c.1339-119T= MANE Select	ENSP00000365891.4:n.1339-119T=
ENST00000376701.4:c.1339-119T=	ENSP00000365891.4:n.1339-119T=
ENST00000470107.1:n.48-119T=
NM_000377.2:c.1339-119T= , LRG_125t1:c.1339-119T=	NP_000368.1:n.1339-119T=
XM_011543977.1:c.1183-119T=	XP_011542279.1:n.1183-119T=
XM_011543977.2:c.1183-119T=	XP_011542279.1:n.1183-119T=
XM_017029786.1:c.1339-119T=	XP_016885275.1:n.1339-119T=
NM_000377.3:c.1339-119T= MANE Select	NP_000368.1:n.1339-119T=