Canonical Allele Identifier: CA2579600725

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688934_48688939del , CM000685.2:g.48688934_48688939del	GRCh38
NC_000023.10:g.48547323_48547328del , CM000685.1:g.48547323_48547328del	GRCh37
NC_000023.9:g.48432267_48432272del	NCBI36
NG_007877.1:g.10138_10143del , LRG_125:g.10138_10143del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.450_455del
ENST00000698625.1:c.1206_1211del	ENSP00000513844.1:p.Pro403_Pro404del
ENST00000698626.1:c.1206_1211del	ENSP00000513845.1:p.Pro403_Pro404del
ENST00000698635.1:c.1206_1211del	ENSP00000513850.1:p.Pro403_Pro404del
ENST00000376701.5:c.1206_1211del MANE Select	ENSP00000365891.4:p.Pro403_Pro404del
ENST00000376701.4:c.1206_1211del	ENSP00000365891.4:p.Pro403_Pro404del
ENST00000474174.1:n.450_455del
NM_000377.2:c.1206_1211del , LRG_125t1:c.1206_1211del	NP_000368.1:p.Pro403_Pro404del
XM_011543977.1:c.1050_1055del	XP_011542279.1:p.Pro351_Pro352del
XM_011543977.2:c.1050_1055del	XP_011542279.1:p.Pro351_Pro352del
XM_017029786.1:c.1206_1211del	XP_016885275.1:p.Pro403_Pro404del
NM_000377.3:c.1206_1211del MANE Select	NP_000368.1:p.Pro403_Pro404del