Canonical Allele Identifier: CA2544846787

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48683854del , CM000685.2:g.48683854del	GRCh38
NC_000023.10:g.48542243del , CM000685.1:g.48542243del	GRCh37
NC_000023.9:g.48427187del	NCBI36
NG_007877.1:g.5058del , LRG_125:g.5058del

Transcript Alleles

HGVS	Amino-acid change
ENST00000483750.6:n.34del
ENST00000698625.1:c.1del	ENSP00000513844.1:p.Met1Ter
ENST00000698626.1:c.1del	ENSP00000513845.1:p.Met1Ter
ENST00000698635.1:c.1del	ENSP00000513850.1:p.Met1Ter
ENST00000376701.5:c.1del MANE Select	ENSP00000365891.4:p.Met1Ter
ENST00000376701.4:c.1del	ENSP00000365891.4:p.Met1Ter
ENST00000450772.5:c.1del	ENSP00000410537.1:p.Met1Ter
ENST00000465982.5:n.36del
ENST00000483750.5:n.27del
NM_000377.2:c.1del , LRG_125t1:c.1del	NP_000368.1:p.Met1Ter
XM_011543977.1:c.1del	XP_011542279.1:p.Met1Ter
XM_011543977.2:c.1del	XP_011542279.1:p.Met1Ter
XM_017029786.1:c.1del	XP_016885275.1:p.Met1Ter
NM_000377.3:c.1del MANE Select	NP_000368.1:p.Met1Ter