Canonical Allele Identifier: CA2695234047
Gene: WAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48688098dup , CM000685.2:g.48688098dup GRCh38
NC_000023.10:g.48546487dup , CM000685.1:g.48546487dup GRCh37
NC_000023.9:g.48431431dup NCBI36
NG_007877.1:g.9302dup , LRG_125:g.9302dup

Transcript Alleles

HGVS Amino-acid change
ENST00000483750.6:n.812dup
ENST00000490627.2:n.216dup
ENST00000698625.1:c.777+2dup ENSP00000513844.1:n.777+2dup
ENST00000698626.1:c.777+2dup ENSP00000513845.1:n.777+2dup
ENST00000698635.1:c.777+2dup ENSP00000513850.1:n.777+2dup
ENST00000376701.5:c.777+2dup MANE Select ENSP00000365891.4:n.777+2dup
ENST00000376701.4:c.777+2dup ENSP00000365891.4:n.777+2dup
ENST00000465982.5:n.679dup
ENST00000483750.5:n.805dup
ENST00000490627.1:n.199dup
NM_000377.2:c.777+2dup , LRG_125t1:c.777+2dup NP_000368.1:n.777+2dup
XM_011543977.1:c.777+2dup XP_011542279.1:n.777+2dup
XM_011543977.2:c.777+2dup XP_011542279.1:n.777+2dup
XM_017029786.1:c.777+2dup XP_016885275.1:n.777+2dup
NM_000377.3:c.777+2dup MANE Select NP_000368.1:n.777+2dup
Search 100 bp 5'
Search 100 bp 3'