Canonical Allele Identifier: CA2695233772

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688803_48688804delinsA , CM000685.2:g.48688803_48688804delinsA	GRCh38
NC_000023.10:g.48547192_48547193delinsA , CM000685.1:g.48547192_48547193delinsA	GRCh37
NC_000023.9:g.48432136_48432137delinsA	NCBI36
NG_007877.1:g.10007_10008delinsA , LRG_125:g.10007_10008delinsA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.319_320delinsA
ENST00000698625.1:c.1075_1076delinsA	ENSP00000513844.1:p.Pro359ThrfsTer?
ENST00000698626.1:c.1075_1076delinsA	ENSP00000513845.1:p.Pro359ThrfsTer?
ENST00000698635.1:c.1075_1076delinsA	ENSP00000513850.1:p.Pro359ThrfsTer?
ENST00000376701.5:c.1075_1076delinsA MANE Select	ENSP00000365891.4:p.Pro359ThrfsTer?
ENST00000376701.4:c.1075_1076delinsA	ENSP00000365891.4:p.Pro359ThrfsTer?
ENST00000474174.1:n.319_320delinsA
NM_000377.2:c.1075_1076delinsA , LRG_125t1:c.1075_1076delinsA	NP_000368.1:p.Pro359ThrfsTer?
XM_011543977.1:c.932-13_932-12delinsA	XP_011542279.1:n.932-13_932-12delinsA
XM_011543977.2:c.932-13_932-12delinsA	XP_011542279.1:n.932-13_932-12delinsA
XM_017029786.1:c.1075_1076delinsA	XP_016885275.1:p.Pro359ThrfsTer?
NM_000377.3:c.1075_1076delinsA MANE Select	NP_000368.1:p.Pro359ThrfsTer?