Canonical Allele Identifier: CA2428355744
Gene: WAS HGNC NCBI

Linked Data

dbSNP Id: rs1557007256

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48688910_48688918dup , CM000685.2:g.48688910_48688918dup GRCh38
NC_000023.10:g.48547299_48547307dup , CM000685.1:g.48547299_48547307dup GRCh37
NC_000023.9:g.48432243_48432251dup NCBI36
NG_007877.1:g.10114_10122dup , LRG_125:g.10114_10122dup

Transcript Alleles

HGVS Amino-acid change
ENST00000474174.2:n.426_434dup
ENST00000698625.1:c.1182_1190dup ENSP00000513844.1:p.Pro397_Pro398insProPr...
ENST00000698626.1:c.1182_1190dup ENSP00000513845.1:p.Pro397_Pro398insProPr...
ENST00000698635.1:c.1182_1190dup ENSP00000513850.1:p.Pro397_Pro398insProPr...
ENST00000376701.5:c.1182_1190dup MANE Select ENSP00000365891.4:p.Pro397_Pro398insProPr...
ENST00000376701.4:c.1182_1190dup ENSP00000365891.4:p.Pro397_Pro398insProPr...
ENST00000474174.1:n.426_434dup
NM_000377.2:c.1182_1190dup , LRG_125t1:c.1182_1190dup NP_000368.1:p.Pro397_Pro398insProProPro
XM_011543977.1:c.1026_1034dup XP_011542279.1:p.Pro345_Pro346insProProPr...
XM_011543977.2:c.1026_1034dup XP_011542279.1:p.Pro345_Pro346insProProPr...
XM_017029786.1:c.1182_1190dup XP_016885275.1:p.Pro397_Pro398insProProPr...
NM_000377.3:c.1182_1190dup MANE Select NP_000368.1:p.Pro397_Pro398insProProPro