Canonical Allele Identifier: CA2739290494
Gene: WAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48688451_48688462del , CM000685.2:g.48688451_48688462del GRCh38
NC_000023.10:g.48546840_48546851del , CM000685.1:g.48546840_48546851del GRCh37
NC_000023.9:g.48431784_48431795del NCBI36
NG_007877.1:g.9655_9666del , LRG_125:g.9655_9666del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474174.2:n.173_175+9del
ENST00000698625.1:c.929_931+9del
ENST00000698626.1:c.929_931+9del
ENST00000698635.1:c.929_931+9del
ENST00000376701.5:c.929_931+9del
ENST00000376701.4:c.929_931+9del
ENST00000474174.1:n.173_175+9del
NM_000377.2:c.929_931+9del , LRG_125t1:c.929_931+9del
XM_011543977.1:c.929_931+9del
XM_011543977.2:c.929_931+9del
XM_017029786.1:c.929_931+9del
NM_000377.3:c.929_931+9del