Canonical Allele Identifier: CA412865387

Gene: WAS

Linked Data

• ClinVar Variation Id: 1447769
• ClinVar RCV Id: RCV001996908
• dbSNP Id: rs1569493676
• MyVariant Identifiers: chrX:g.48542294G>A (hg19) ; chrX:g.48683905G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48683905G>A , CM000685.2:g.48683905G>A	GRCh38
NC_000023.10:g.48542294G>A , CM000685.1:g.48542294G>A	GRCh37
NC_000023.9:g.48427238G>A	NCBI36
NG_007877.1:g.5109G>A , LRG_125:g.5109G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.85G>A
ENST00000698625.1:c.52G>A	ENSP00000513844.1:p.Val18Ile
ENST00000698626.1:c.52G>A	ENSP00000513845.1:p.Val18Ile
ENST00000698635.1:c.52G>A	ENSP00000513850.1:p.Val18Ile
ENST00000376701.5:c.52G>A MANE Select	ENSP00000365891.4:p.Val18Ile
ENST00000376701.4:c.52G>A	ENSP00000365891.4:p.Val18Ile
ENST00000450772.5:c.52G>A	ENSP00000410537.1:p.Val18Ile
ENST00000465982.5:n.87G>A
ENST00000483750.5:n.78G>A
NM_000377.2:c.52G>A , LRG_125t1:c.52G>A	NP_000368.1:p.Val18Ile
XM_011543977.1:c.52G>A	XP_011542279.1:p.Val18Ile
XM_011543977.2:c.52G>A	XP_011542279.1:p.Val18Ile
XM_017029786.1:c.52G>A	XP_016885275.1:p.Val18Ile
NM_000377.3:c.52G>A MANE Select	NP_000368.1:p.Val18Ile