Canonical Allele Identifier: CA2499214011

Gene: WAS

Linked Data

• gnomAD v4: X-48688898-GCCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688901_48688903del , CM000685.2:g.48688901_48688903del	GRCh38
NC_000023.10:g.48547290_48547292del , CM000685.1:g.48547290_48547292del	GRCh37
NC_000023.9:g.48432234_48432236del	NCBI36
NG_007877.1:g.10105_10107del , LRG_125:g.10105_10107del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.417_419del
ENST00000698625.1:c.1173_1175del	ENSP00000513844.1:p.Pro392del
ENST00000698626.1:c.1173_1175del	ENSP00000513845.1:p.Pro392del
ENST00000698635.1:c.1173_1175del	ENSP00000513850.1:p.Pro392del
ENST00000376701.5:c.1173_1175del MANE Select	ENSP00000365891.4:p.Pro392del
ENST00000376701.4:c.1173_1175del	ENSP00000365891.4:p.Pro392del
ENST00000474174.1:n.417_419del
NM_000377.2:c.1173_1175del , LRG_125t1:c.1173_1175del	NP_000368.1:p.Pro392del
XM_011543977.1:c.1017_1019del	XP_011542279.1:p.Pro340del
XM_011543977.2:c.1017_1019del	XP_011542279.1:p.Pro340del
XM_017029786.1:c.1173_1175del	XP_016885275.1:p.Pro392del
NM_000377.3:c.1173_1175del MANE Select	NP_000368.1:p.Pro392del