Canonical Allele Identifier: CA916081268

Gene: WAS

Linked Data

• ClinVar Variation Id: 861115
• ClinVar RCV Id: RCV001067557
• dbSNP Id: rs1557007165

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688786dup , CM000685.2:g.48688786dup	GRCh38
NC_000023.10:g.48547175dup , CM000685.1:g.48547175dup	GRCh37
NC_000023.9:g.48432119dup	NCBI36
NG_007877.1:g.9990dup , LRG_125:g.9990dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.302dup
ENST00000698625.1:c.1058dup	ENSP00000513844.1:p.Pro354ThrfsTer?
ENST00000698626.1:c.1058dup	ENSP00000513845.1:p.Pro354ThrfsTer?
ENST00000698635.1:c.1058dup	ENSP00000513850.1:p.Pro354ThrfsTer?
ENST00000376701.5:c.1058dup MANE Select	ENSP00000365891.4:p.Pro354ThrfsTer?
ENST00000376701.4:c.1058dup	ENSP00000365891.4:p.Pro354ThrfsTer?
ENST00000474174.1:n.302dup
NM_000377.2:c.1058dup , LRG_125t1:c.1058dup	NP_000368.1:p.Pro354ThrfsTer?
XM_011543977.1:c.932-30dup	XP_011542279.1:n.932-30dup
XM_011543977.2:c.932-30dup	XP_011542279.1:n.932-30dup
XM_017029786.1:c.1058dup	XP_016885275.1:p.Pro354ThrfsTer?
NM_000377.3:c.1058dup MANE Select	NP_000368.1:p.Pro354ThrfsTer?