Canonical Allele Identifier: CA10404075

Gene: WAS

Linked Data

• ClinVar Variation Id: 2923090
• ClinVar RCV Id: RCV003780208
• dbSNP Id: rs782303232
• ExAC: X:48547468 A / T
• gnomAD v2: X-48547468-A-T
• gnomAD v3: X-48689079-A-T
• gnomAD v4: X-48689079-A-T
• MyVariant Identifiers: chrX:g.48547468A>T (hg19) ; chrX:g.48689079A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48689079A>T , CM000685.2:g.48689079A>T	GRCh38
NC_000023.10:g.48547468A>T , CM000685.1:g.48547468A>T	GRCh37
NC_000023.9:g.48432412A>T	NCBI36
NG_007877.1:g.10283A>T , LRG_125:g.10283A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.582+13A>T
ENST00000698625.1:c.1338+13A>T	ENSP00000513844.1:n.1338+13A>T
ENST00000698626.1:c.1338+13A>T	ENSP00000513845.1:n.1338+13A>T
ENST00000698635.1:c.1338+13A>T	ENSP00000513850.1:n.1338+13A>T
ENST00000376701.5:c.1338+13A>T MANE Select	ENSP00000365891.4:n.1338+13A>T
ENST00000376701.4:c.1338+13A>T	ENSP00000365891.4:n.1338+13A>T
ENST00000470107.1:n.47+13A>T
NM_000377.2:c.1338+13A>T , LRG_125t1:c.1338+13A>T	NP_000368.1:n.1338+13A>T
XM_011543977.1:c.1182+13A>T	XP_011542279.1:n.1182+13A>T
XM_011543977.2:c.1182+13A>T	XP_011542279.1:n.1182+13A>T
XM_017029786.1:c.1338+13A>T	XP_016885275.1:n.1338+13A>T
NM_000377.3:c.1338+13A>T MANE Select	NP_000368.1:n.1338+13A>T