Canonical Allele Identifier: CA412867622
Community Standard Title: NM_000377.3(WAS):c.397G>A (p.Glu133Lys)
Gene: WAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48685770G>A , CM000685.2:g.48685770G>A GRCh38
NC_000023.10:g.48544159G>A , CM000685.1:g.48544159G>A GRCh37
NC_000023.9:g.48429103G>A NCBI36
NG_007877.1:g.6974G>A , LRG_125:g.6974G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000377.3:c.397G>A MANE Select NP_000368.1:p.Glu133Lys
ENST00000376701.5:c.397G>A MANE Select ENSP00000365891.4:p.Glu133Lys
NM_000377.2:c.397G>A , LRG_125t1:c.397G>A NP_000368.1:p.Glu133Lys
ENST00000376701.4:c.397G>A ENSP00000365891.4:p.Glu133Lys
ENST00000450772.5:c.397G>A ENSP00000410537.1:p.Glu133Lys
ENST00000465982.5:n.432G>A
ENST00000483750.5:n.423G>A
ENST00000483750.6:n.430G>A
ENST00000490627.2:n.9G>A
ENST00000698625.1:c.397G>A ENSP00000513844.1:p.Glu133Lys
ENST00000698626.1:c.397G>A ENSP00000513845.1:p.Glu133Lys
ENST00000698635.1:c.397G>A ENSP00000513850.1:p.Glu133Lys
XM_011543977.1:c.397G>A XP_011542279.1:p.Glu133Lys
XM_011543977.2:c.397G>A XP_011542279.1:p.Glu133Lys
XM_017029786.1:c.397G>A XP_016885275.1:p.Glu133Lys