Canonical Allele Identifier: CA2428355853

Gene: WAS

Linked Data

• dbSNP Id: rs2062431693

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48689141_48689160dup , CM000685.2:g.48689141_48689160dup	GRCh38
NC_000023.10:g.48547530_48547549dup , CM000685.1:g.48547530_48547549dup	GRCh37
NC_000023.9:g.48432474_48432493dup	NCBI36
NG_007877.1:g.10345_10364dup , LRG_125:g.10345_10364dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.582+75_582+94dup
ENST00000698625.1:c.1338+75_1338+94dup	ENSP00000513844.1:n.1338+75_1338+94dup
ENST00000698626.1:c.1338+75_1338+94dup	ENSP00000513845.1:n.1338+75_1338+94dup
ENST00000698635.1:c.1338+75_1338+94dup	ENSP00000513850.1:n.1338+75_1338+94dup
ENST00000376701.5:c.1338+75_1338+94dup MANE Select	ENSP00000365891.4:n.1338+75_1338+94dup
ENST00000376701.4:c.1338+75_1338+94dup	ENSP00000365891.4:n.1338+75_1338+94dup
ENST00000470107.1:n.47+75_47+94dup
NM_000377.2:c.1338+75_1338+94dup , LRG_125t1:c.1338+75_1338+94dup	NP_000368.1:n.1338+75_1338+94dup
XM_011543977.1:c.1182+75_1182+94dup	XP_011542279.1:n.1182+75_1182+94dup
XM_011543977.2:c.1182+75_1182+94dup	XP_011542279.1:n.1182+75_1182+94dup
XM_017029786.1:c.1338+75_1338+94dup	XP_016885275.1:n.1338+75_1338+94dup
NM_000377.3:c.1338+75_1338+94dup MANE Select	NP_000368.1:n.1338+75_1338+94dup