Canonical Allele Identifier: CA2693644988

Gene: WAS

Linked Data

• gnomAD v4: X-48688922-ACCACCG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688931_48688936del , CM000685.2:g.48688931_48688936del	GRCh38
NC_000023.10:g.48547320_48547325del , CM000685.1:g.48547320_48547325del	GRCh37
NC_000023.9:g.48432264_48432269del	NCBI36
NG_007877.1:g.10135_10140del , LRG_125:g.10135_10140del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.447_452del
ENST00000698625.1:c.1203_1208del	ENSP00000513844.1:p.Pro402_Pro403del
ENST00000698626.1:c.1203_1208del	ENSP00000513845.1:p.Pro402_Pro403del
ENST00000698635.1:c.1203_1208del	ENSP00000513850.1:p.Pro402_Pro403del
ENST00000376701.5:c.1203_1208del MANE Select	ENSP00000365891.4:p.Pro402_Pro403del
ENST00000376701.4:c.1203_1208del	ENSP00000365891.4:p.Pro402_Pro403del
ENST00000474174.1:n.447_452del
NM_000377.2:c.1203_1208del , LRG_125t1:c.1203_1208del	NP_000368.1:p.Pro402_Pro403del
XM_011543977.1:c.1047_1052del	XP_011542279.1:p.Pro350_Pro351del
XM_011543977.2:c.1047_1052del	XP_011542279.1:p.Pro350_Pro351del
XM_017029786.1:c.1203_1208del	XP_016885275.1:p.Pro402_Pro403del
NM_000377.3:c.1203_1208del MANE Select	NP_000368.1:p.Pro402_Pro403del