Canonical Allele Identifier: CA645619092

Gene: WAS

Linked Data

• COSMIC: COSM5701714

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688724_48688725delinsCT , CM000685.2:g.48688724_48688725delinsCT	GRCh38
NC_000023.10:g.48547113_48547114delinsCT , CM000685.1:g.48547113_48547114delinsCT	GRCh37
NC_000023.9:g.48432057_48432058delinsCT	NCBI36
NG_007877.1:g.9928_9929delinsCT , LRG_125:g.9928_9929delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.240_241delinsCT
ENST00000698625.1:c.996_997delinsCT	ENSP00000513844.1:p.Gly333Trp
ENST00000698626.1:c.996_997delinsCT	ENSP00000513845.1:p.Gly333Trp
ENST00000698635.1:c.996_997delinsCT	ENSP00000513850.1:p.Gly333Trp
ENST00000376701.5:c.996_997delinsCT MANE Select	ENSP00000365891.4:p.Gly333Trp
ENST00000376701.4:c.996_997delinsCT	ENSP00000365891.4:p.Gly333Trp
ENST00000474174.1:n.240_241delinsCT
NM_000377.2:c.996_997delinsCT , LRG_125t1:c.996_997delinsCT	NP_000368.1:p.Gly333Trp
XM_011543977.1:c.932-92_932-91delinsCT	XP_011542279.1:n.932-92_932-91delinsCT
XM_011543977.2:c.932-92_932-91delinsCT	XP_011542279.1:n.932-92_932-91delinsCT
XM_017029786.1:c.996_997delinsCT	XP_016885275.1:p.Gly333Trp
NM_000377.3:c.996_997delinsCT MANE Select	NP_000368.1:p.Gly333Trp