Canonical Allele Identifier: CA2579600561
Gene: WAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48683790del , CM000685.2:g.48683790del GRCh38
NC_000023.10:g.48542179del , CM000685.1:g.48542179del GRCh37
NC_000023.9:g.48427123del NCBI36
NG_007877.1:g.4994del , LRG_125:g.4994del

Transcript Alleles

HGVS Amino-acid change
ENST00000698625.1:c.-34-30del ENSP00000513844.1:n.-34-30del
ENST00000376701.4:c.-64del ENSP00000365891.4:n.-64del
ENST00000450772.5:c.-34-30del ENSP00000410537.1:n.-34-30del
XM_011543977.1:c.-64del XP_011542279.1:n.-64del
XM_017029786.1:c.-64del XP_016885275.1:n.-64del