Canonical Allele Identifier: CA2428354219

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48684015G= , CM000685.2:g.48684015G=	GRCh38
NC_000023.10:g.48542404G= , CM000685.1:g.48542404G=	GRCh37
NC_000023.9:g.48427348G=	NCBI36
NG_007877.1:g.5219G= , LRG_125:g.5219G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.165+30G=
ENST00000698625.1:c.132+30G=	ENSP00000513844.1:n.132+30G=
ENST00000698626.1:c.132+30G=	ENSP00000513845.1:n.132+30G=
ENST00000698635.1:c.132+30G=	ENSP00000513850.1:n.132+30G=
ENST00000376701.5:c.132+30G= MANE Select	ENSP00000365891.4:n.132+30G=
ENST00000376701.4:c.132+30G=	ENSP00000365891.4:n.132+30G=
ENST00000450772.5:c.132+30G=	ENSP00000410537.1:n.132+30G=
ENST00000465982.5:n.167+30G=
ENST00000483750.5:n.158+30G=
NM_000377.2:c.132+30G= , LRG_125t1:c.132+30G=	NP_000368.1:n.132+30G=
XM_011543977.1:c.132+30G=	XP_011542279.1:n.132+30G=
XM_011543977.2:c.132+30G=	XP_011542279.1:n.132+30G=
XM_017029786.1:c.132+30G=	XP_016885275.1:n.132+30G=
NM_000377.3:c.132+30G= MANE Select	NP_000368.1:n.132+30G=