Canonical Allele Identifier: CA10403968

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48686927G>A , CM000685.2:g.48686927G>A	GRCh38
NC_000023.10:g.48545316G>A , CM000685.1:g.48545316G>A	GRCh37
NC_000023.9:g.48430260G>A	NCBI36
NG_007877.1:g.8131G>A , LRG_125:g.8131G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000377.3:c.706G>A MANE Select	NP_000368.1:p.Ala236Thr
ENST00000376701.5:c.706G>A MANE Select	ENSP00000365891.4:p.Ala236Thr
NM_000377.2:c.706G>A , LRG_125t1:c.706G>A	NP_000368.1:p.Ala236Thr
ENST00000376701.4:c.706G>A	ENSP00000365891.4:p.Ala236Thr
ENST00000465982.5:n.606G>A
ENST00000483750.5:n.732G>A
ENST00000483750.6:n.739G>A
ENST00000490627.1:n.154+793G>A
ENST00000490627.2:n.171+793G>A
ENST00000698625.1:c.706G>A	ENSP00000513844.1:p.Ala236Thr
ENST00000698626.1:c.706G>A	ENSP00000513845.1:p.Ala236Thr
ENST00000698635.1:c.706G>A	ENSP00000513850.1:p.Ala236Thr
XM_011543977.1:c.706G>A	XP_011542279.1:p.Ala236Thr
XM_011543977.2:c.706G>A	XP_011542279.1:p.Ala236Thr
XM_017029786.1:c.706G>A	XP_016885275.1:p.Ala236Thr