Canonical Allele Identifier: CA2428355659

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688729G= , CM000685.2:g.48688729G=	GRCh38
NC_000023.10:g.48547118G= , CM000685.1:g.48547118G=	GRCh37
NC_000023.9:g.48432062G=	NCBI36
NG_007877.1:g.9933G= , LRG_125:g.9933G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.245G=
ENST00000698625.1:c.1001G=	ENSP00000513844.1:p.Gly334=
ENST00000698626.1:c.1001G=	ENSP00000513845.1:p.Gly334=
ENST00000698635.1:c.1001G=	ENSP00000513850.1:p.Gly334=
ENST00000376701.5:c.1001G= MANE Select	ENSP00000365891.4:p.Gly334=
ENST00000376701.4:c.1001G=	ENSP00000365891.4:p.Gly334=
ENST00000474174.1:n.245G=
NM_000377.2:c.1001G= , LRG_125t1:c.1001G=	NP_000368.1:p.Gly334=
XM_011543977.1:c.932-87G=	XP_011542279.1:n.932-87G=
XM_011543977.2:c.932-87G=	XP_011542279.1:n.932-87G=
XM_017029786.1:c.1001G=	XP_016885275.1:p.Gly334=
NM_000377.3:c.1001G= MANE Select	NP_000368.1:p.Gly334=