Canonical Allele Identifier: CA2428355569

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688474G= , CM000685.2:g.48688474G=	GRCh38
NC_000023.10:g.48546863G= , CM000685.1:g.48546863G=	GRCh37
NC_000023.9:g.48431807G=	NCBI36
NG_007877.1:g.9678G= , LRG_125:g.9678G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.175+21G=
ENST00000698625.1:c.931+21G=	ENSP00000513844.1:n.931+21G=
ENST00000698626.1:c.931+21G=	ENSP00000513845.1:n.931+21G=
ENST00000698635.1:c.931+21G=	ENSP00000513850.1:n.931+21G=
ENST00000376701.5:c.931+21G= MANE Select	ENSP00000365891.4:n.931+21G=
ENST00000376701.4:c.931+21G=	ENSP00000365891.4:n.931+21G=
ENST00000474174.1:n.175+21G=
NM_000377.2:c.931+21G= , LRG_125t1:c.931+21G=	NP_000368.1:n.931+21G=
XM_011543977.1:c.931+21G=	XP_011542279.1:n.931+21G=
XM_011543977.2:c.931+21G=	XP_011542279.1:n.931+21G=
XM_017029786.1:c.931+21G=	XP_016885275.1:n.931+21G=
NM_000377.3:c.931+21G= MANE Select	NP_000368.1:n.931+21G=