Canonical Allele Identifier: CA2693645043

Gene: WAS

Linked Data

• gnomAD v4: X-48688964-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688969del , CM000685.2:g.48688969del	GRCh38
NC_000023.10:g.48547358del , CM000685.1:g.48547358del	GRCh37
NC_000023.9:g.48432302del	NCBI36
NG_007877.1:g.10173del , LRG_125:g.10173del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.485del
ENST00000698625.1:c.1241del	ENSP00000513844.1:p.Pro414HisfsTer?
ENST00000698626.1:c.1241del	ENSP00000513845.1:p.Pro414HisfsTer?
ENST00000698635.1:c.1241del	ENSP00000513850.1:p.Pro414HisfsTer?
ENST00000376701.5:c.1241del MANE Select	ENSP00000365891.4:p.Pro414HisfsTer?
ENST00000376701.4:c.1241del	ENSP00000365891.4:p.Pro414HisfsTer?
ENST00000474174.1:n.485del
NM_000377.2:c.1241del , LRG_125t1:c.1241del	NP_000368.1:p.Pro414HisfsTer?
XM_011543977.1:c.1085del	XP_011542279.1:p.Pro362HisfsTer?
XM_011543977.2:c.1085del	XP_011542279.1:p.Pro362HisfsTer?
XM_017029786.1:c.1241del	XP_016885275.1:p.Pro414HisfsTer?
NM_000377.3:c.1241del MANE Select	NP_000368.1:p.Pro414HisfsTer?