Canonical Allele Identifier: CA2579600670
Gene: WAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48688015G>A , CM000685.2:g.48688015G>A GRCh38
NC_000023.10:g.48546404G>A , CM000685.1:g.48546404G>A GRCh37
NC_000023.9:g.48431348G>A NCBI36
NG_007877.1:g.9219G>A , LRG_125:g.9219G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000483750.6:n.768-39G>A
ENST00000490627.2:n.172-39G>A
ENST00000698625.1:c.735-39G>A ENSP00000513844.1:n.735-39G>A
ENST00000698626.1:c.735-39G>A ENSP00000513845.1:n.735-39G>A
ENST00000698635.1:c.735-39G>A ENSP00000513850.1:n.735-39G>A
ENST00000376701.5:c.735-39G>A MANE Select ENSP00000365891.4:n.735-39G>A
ENST00000376701.4:c.735-39G>A ENSP00000365891.4:n.735-39G>A
ENST00000465982.5:n.635-39G>A
ENST00000483750.5:n.761-39G>A
ENST00000490627.1:n.155-39G>A
NM_000377.2:c.735-39G>A , LRG_125t1:c.735-39G>A NP_000368.1:n.735-39G>A
XM_011543977.1:c.735-39G>A XP_011542279.1:n.735-39G>A
XM_011543977.2:c.735-39G>A XP_011542279.1:n.735-39G>A
XM_017029786.1:c.735-39G>A XP_016885275.1:n.735-39G>A
NM_000377.3:c.735-39G>A MANE Select NP_000368.1:n.735-39G>A
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