Canonical Allele Identifier: CA2693644933
Gene: WAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48688907_48688912dup , CM000685.2:g.48688907_48688912dup GRCh38
NC_000023.10:g.48547296_48547301dup , CM000685.1:g.48547296_48547301dup GRCh37
NC_000023.9:g.48432240_48432245dup NCBI36
NG_007877.1:g.10111_10116dup , LRG_125:g.10111_10116dup

Transcript Alleles

HGVS Amino-acid change
ENST00000474174.2:n.423_428dup
ENST00000698625.1:c.1179_1184dup ENSP00000513844.1:p.Pro395_Pro396insProPr...
ENST00000698626.1:c.1179_1184dup ENSP00000513845.1:p.Pro395_Pro396insProPr...
ENST00000698635.1:c.1179_1184dup ENSP00000513850.1:p.Pro395_Pro396insProPr...
ENST00000376701.5:c.1179_1184dup MANE Select ENSP00000365891.4:p.Pro395_Pro396insProPr...
ENST00000376701.4:c.1179_1184dup ENSP00000365891.4:p.Pro395_Pro396insProPr...
ENST00000474174.1:n.423_428dup
NM_000377.2:c.1179_1184dup , LRG_125t1:c.1179_1184dup NP_000368.1:p.Pro395_Pro396insProPro
XM_011543977.1:c.1023_1028dup XP_011542279.1:p.Pro343_Pro344insProPro
XM_011543977.2:c.1023_1028dup XP_011542279.1:p.Pro343_Pro344insProPro
XM_017029786.1:c.1179_1184dup XP_016885275.1:p.Pro395_Pro396insProPro
NM_000377.3:c.1179_1184dup MANE Select NP_000368.1:p.Pro395_Pro396insProPro