Canonical Allele Identifier: CA1139532693
Gene: WAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48683844_48683995del , CM000685.2:g.48683844_48683995del GRCh38
NC_000023.10:g.48542233_48542384del , CM000685.1:g.48542233_48542384del GRCh37
NC_000023.9:g.48427177_48427328del NCBI36
NG_007877.1:g.5048_5199del , LRG_125:g.5048_5199del

Transcript Alleles

HGVS Amino-acid change
ENST00000483750.6:n.24_165+10del
ENST00000698625.1:c.-10_132+10del
ENST00000698626.1:c.-10_132+10del
ENST00000698635.1:c.-10_132+10del
ENST00000376701.5:c.-10_132+10del
ENST00000376701.4:c.-10_132+10del
ENST00000450772.5:c.-10_132+10del
ENST00000465982.5:n.26_167+10del
ENST00000483750.5:n.17_158+10del
NM_000377.2:c.-10_132+10del , LRG_125t1:c.-10_132+10del
XM_011543977.1:c.-10_132+10del
XM_011543977.2:c.-10_132+10del
XM_017029786.1:c.-10_132+10del
NM_000377.3:c.-10_132+10del