Canonical Allele Identifier: CA2428354182

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48683909A= , CM000685.2:g.48683909A=	GRCh38
NC_000023.10:g.48542298A= , CM000685.1:g.48542298A=	GRCh37
NC_000023.9:g.48427242A=	NCBI36
NG_007877.1:g.5113A= , LRG_125:g.5113A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.89A=
ENST00000698625.1:c.56A=	ENSP00000513844.1:p.Gln19=
ENST00000698626.1:c.56A=	ENSP00000513845.1:p.Gln19=
ENST00000698635.1:c.56A=	ENSP00000513850.1:p.Gln19=
ENST00000376701.5:c.56A= MANE Select	ENSP00000365891.4:p.Gln19=
ENST00000376701.4:c.56A=	ENSP00000365891.4:p.Gln19=
ENST00000450772.5:c.56A=	ENSP00000410537.1:p.Gln19=
ENST00000465982.5:n.91A=
ENST00000483750.5:n.82A=
NM_000377.2:c.56A= , LRG_125t1:c.56A=	NP_000368.1:p.Gln19=
XM_011543977.1:c.56A=	XP_011542279.1:p.Gln19=
XM_011543977.2:c.56A=	XP_011542279.1:p.Gln19=
XM_017029786.1:c.56A=	XP_016885275.1:p.Gln19=
NM_000377.3:c.56A= MANE Select	NP_000368.1:p.Gln19=