Canonical Allele Identifier: CA2428355677

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688792C= , CM000685.2:g.48688792C=	GRCh38
NC_000023.10:g.48547181C= , CM000685.1:g.48547181C=	GRCh37
NC_000023.9:g.48432125C=	NCBI36
NG_007877.1:g.9996C= , LRG_125:g.9996C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.308C=
ENST00000698625.1:c.1064C=	ENSP00000513844.1:p.Thr355=
ENST00000698626.1:c.1064C=	ENSP00000513845.1:p.Thr355=
ENST00000698635.1:c.1064C=	ENSP00000513850.1:p.Thr355=
ENST00000376701.5:c.1064C= MANE Select	ENSP00000365891.4:p.Thr355=
ENST00000376701.4:c.1064C=	ENSP00000365891.4:p.Thr355=
ENST00000474174.1:n.308C=
NM_000377.2:c.1064C= , LRG_125t1:c.1064C=	NP_000368.1:p.Thr355=
XM_011543977.1:c.932-24C=	XP_011542279.1:n.932-24C=
XM_011543977.2:c.932-24C=	XP_011542279.1:n.932-24C=
XM_017029786.1:c.1064C=	XP_016885275.1:p.Thr355=
NM_000377.3:c.1064C= MANE Select	NP_000368.1:p.Thr355=