Canonical Allele Identifier: CA412872029

Gene: WAS

Linked Data

• ClinVar Variation Id: 638575
• ClinVar RCV Id: RCV000791261
• dbSNP Id: rs1602178800
• MyVariant Identifiers: chrX:g.48546441A>G (hg19) ; chrX:g.48688052A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688052A>G , CM000685.2:g.48688052A>G	GRCh38
NC_000023.10:g.48546441A>G , CM000685.1:g.48546441A>G	GRCh37
NC_000023.9:g.48431385A>G	NCBI36
NG_007877.1:g.9256A>G , LRG_125:g.9256A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.768-2A>G
ENST00000490627.2:n.172-2A>G
ENST00000698625.1:c.735-2A>G	ENSP00000513844.1:n.735-2A>G
ENST00000698626.1:c.735-2A>G	ENSP00000513845.1:n.735-2A>G
ENST00000698635.1:c.735-2A>G	ENSP00000513850.1:n.735-2A>G
ENST00000376701.5:c.735-2A>G MANE Select	ENSP00000365891.4:n.735-2A>G
ENST00000376701.4:c.735-2A>G	ENSP00000365891.4:n.735-2A>G
ENST00000465982.5:n.635-2A>G
ENST00000483750.5:n.761-2A>G
ENST00000490627.1:n.155-2A>G
NM_000377.2:c.735-2A>G , LRG_125t1:c.735-2A>G	NP_000368.1:n.735-2A>G
XM_011543977.1:c.735-2A>G	XP_011542279.1:n.735-2A>G
XM_011543977.2:c.735-2A>G	XP_011542279.1:n.735-2A>G
XM_017029786.1:c.735-2A>G	XP_016885275.1:n.735-2A>G
NM_000377.3:c.735-2A>G MANE Select	NP_000368.1:n.735-2A>G