Canonical Allele Identifier: CA2428355440
Gene: WAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48687997T= , CM000685.2:g.48687997T= GRCh38
NC_000023.10:g.48546386T= , CM000685.1:g.48546386T= GRCh37
NC_000023.9:g.48431330T= NCBI36
NG_007877.1:g.9201T= , LRG_125:g.9201T=

Transcript Alleles

HGVS Amino-acid change
ENST00000483750.6:n.768-57T=
ENST00000490627.2:n.172-57T=
ENST00000698625.1:c.735-57T= ENSP00000513844.1:n.735-57T=
ENST00000698626.1:c.735-57T= ENSP00000513845.1:n.735-57T=
ENST00000698635.1:c.735-57T= ENSP00000513850.1:n.735-57T=
ENST00000376701.5:c.735-57T= MANE Select ENSP00000365891.4:n.735-57T=
ENST00000376701.4:c.735-57T= ENSP00000365891.4:n.735-57T=
ENST00000465982.5:n.635-57T=
ENST00000483750.5:n.761-57T=
ENST00000490627.1:n.155-57T=
NM_000377.2:c.735-57T= , LRG_125t1:c.735-57T= NP_000368.1:n.735-57T=
XM_011543977.1:c.735-57T= XP_011542279.1:n.735-57T=
XM_011543977.2:c.735-57T= XP_011542279.1:n.735-57T=
XM_017029786.1:c.735-57T= XP_016885275.1:n.735-57T=
NM_000377.3:c.735-57T= MANE Select NP_000368.1:n.735-57T=