Canonical Allele Identifier: CA2579600722
Gene: WAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48688829_48688831del , CM000685.2:g.48688829_48688831del GRCh38
NC_000023.10:g.48547218_48547220del , CM000685.1:g.48547218_48547220del GRCh37
NC_000023.9:g.48432162_48432164del NCBI36
NG_007877.1:g.10033_10035del , LRG_125:g.10033_10035del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474174.2:n.345_347del
ENST00000698625.1:c.1101_1103del ENSP00000513844.1:p.Pro368del
ENST00000698626.1:c.1101_1103del ENSP00000513845.1:p.Pro368del
ENST00000698635.1:c.1101_1103del ENSP00000513850.1:p.Pro368del
ENST00000376701.5:c.1101_1103del MANE Select ENSP00000365891.4:p.Pro368del
ENST00000376701.4:c.1101_1103del ENSP00000365891.4:p.Pro368del
ENST00000474174.1:n.345_347del
NM_000377.2:c.1101_1103del , LRG_125t1:c.1101_1103del NP_000368.1:p.Pro368del
XM_011543977.1:c.945_947del XP_011542279.1:p.Pro316del
XM_011543977.2:c.945_947del XP_011542279.1:p.Pro316del
XM_017029786.1:c.1101_1103del XP_016885275.1:p.Pro368del
NM_000377.3:c.1101_1103del MANE Select NP_000368.1:p.Pro368del