Canonical Allele Identifier: CA2738505179
Gene: WAS HGNC NCBI

Linked Data

dbSNP Id: rs2147266730
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48688913del , CM000685.2:g.48688913del GRCh38
NC_000023.10:g.48547302del , CM000685.1:g.48547302del GRCh37
NC_000023.9:g.48432246del NCBI36
NG_007877.1:g.10117del , LRG_125:g.10117del

Transcript Alleles

HGVS Amino-acid change
ENST00000474174.2:n.429del
ENST00000698625.1:c.1185del ENSP00000513844.1:p.Pro396HisfsTer?
ENST00000698626.1:c.1185del ENSP00000513845.1:p.Pro396HisfsTer?
ENST00000698635.1:c.1185del ENSP00000513850.1:p.Pro396HisfsTer?
ENST00000376701.5:c.1185del MANE Select ENSP00000365891.4:p.Pro396HisfsTer?
ENST00000376701.4:c.1185del ENSP00000365891.4:p.Pro396HisfsTer?
ENST00000474174.1:n.429del
NM_000377.2:c.1185del , LRG_125t1:c.1185del NP_000368.1:p.Pro396HisfsTer?
XM_011543977.1:c.1029del XP_011542279.1:p.Pro344HisfsTer?
XM_011543977.2:c.1029del XP_011542279.1:p.Pro344HisfsTer?
XM_017029786.1:c.1185del XP_016885275.1:p.Pro396HisfsTer?
NM_000377.3:c.1185del MANE Select NP_000368.1:p.Pro396HisfsTer?
Search 100 bp 5'
Search 100 bp 3'