Canonical Allele Identifier: CA2428355441
Gene: WAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48688005G= , CM000685.2:g.48688005G= GRCh38
NC_000023.10:g.48546394G= , CM000685.1:g.48546394G= GRCh37
NC_000023.9:g.48431338G= NCBI36
NG_007877.1:g.9209G= , LRG_125:g.9209G=

Transcript Alleles

HGVS Amino-acid change
ENST00000483750.6:n.768-49G=
ENST00000490627.2:n.172-49G=
ENST00000698625.1:c.735-49G= ENSP00000513844.1:n.735-49G=
ENST00000698626.1:c.735-49G= ENSP00000513845.1:n.735-49G=
ENST00000698635.1:c.735-49G= ENSP00000513850.1:n.735-49G=
ENST00000376701.5:c.735-49G= MANE Select ENSP00000365891.4:n.735-49G=
ENST00000376701.4:c.735-49G= ENSP00000365891.4:n.735-49G=
ENST00000465982.5:n.635-49G=
ENST00000483750.5:n.761-49G=
ENST00000490627.1:n.155-49G=
NM_000377.2:c.735-49G= , LRG_125t1:c.735-49G= NP_000368.1:n.735-49G=
XM_011543977.1:c.735-49G= XP_011542279.1:n.735-49G=
XM_011543977.2:c.735-49G= XP_011542279.1:n.735-49G=
XM_017029786.1:c.735-49G= XP_016885275.1:n.735-49G=
NM_000377.3:c.735-49G= MANE Select NP_000368.1:n.735-49G=