Canonical Allele Identifier: CA2740092136
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2944256
ClinVar RCV Id: RCV003806006

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48688907_48688915dup , CM000685.2:g.48688907_48688915dup GRCh38
NC_000023.10:g.48547296_48547304dup , CM000685.1:g.48547296_48547304dup GRCh37
NC_000023.9:g.48432240_48432248dup NCBI36
NG_007877.1:g.10111_10119dup , LRG_125:g.10111_10119dup

Transcript Alleles

HGVS Amino-acid change
ENST00000474174.2:n.423_431dup
ENST00000698625.1:c.1179_1187dup ENSP00000513844.1:p.Pro396_Pro397insProPr...
ENST00000698626.1:c.1179_1187dup ENSP00000513845.1:p.Pro396_Pro397insProPr...
ENST00000698635.1:c.1179_1187dup ENSP00000513850.1:p.Pro396_Pro397insProPr...
ENST00000376701.5:c.1179_1187dup MANE Select ENSP00000365891.4:p.Pro396_Pro397insProPr...
ENST00000376701.4:c.1179_1187dup ENSP00000365891.4:p.Pro396_Pro397insProPr...
ENST00000474174.1:n.423_431dup
NM_000377.2:c.1179_1187dup , LRG_125t1:c.1179_1187dup NP_000368.1:p.Pro396_Pro397insProProPro
XM_011543977.1:c.1023_1031dup XP_011542279.1:p.Pro344_Pro345insProProPr...
XM_011543977.2:c.1023_1031dup XP_011542279.1:p.Pro344_Pro345insProProPr...
XM_017029786.1:c.1179_1187dup XP_016885275.1:p.Pro396_Pro397insProProPr...
NM_000377.3:c.1179_1187dup MANE Select NP_000368.1:p.Pro396_Pro397insProProPro