Canonical Allele Identifier: CA412872144

Gene: WAS

Linked Data

• ClinVar Variation Id: 1526129
• ClinVar RCV Id: RCV002052149
• dbSNP Id: rs2147265861
• MyVariant Identifiers: chrX:g.48546688G>A (hg19) ; chrX:g.48688299G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688299G>A , CM000685.2:g.48688299G>A	GRCh38
NC_000023.10:g.48546688G>A , CM000685.1:g.48546688G>A	GRCh37
NC_000023.9:g.48431632G>A	NCBI36
NG_007877.1:g.9503G>A , LRG_125:g.9503G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.21G>A
ENST00000483750.6:n.1013G>A
ENST00000698625.1:c.778-1G>A	ENSP00000513844.1:n.778-1G>A
ENST00000698626.1:c.778-1G>A	ENSP00000513845.1:n.778-1G>A
ENST00000698635.1:c.778-1G>A	ENSP00000513850.1:n.778-1G>A
ENST00000376701.5:c.778-1G>A MANE Select	ENSP00000365891.4:n.778-1G>A
ENST00000376701.4:c.778-1G>A	ENSP00000365891.4:n.778-1G>A
ENST00000474174.1:n.21G>A
NM_000377.2:c.778-1G>A , LRG_125t1:c.778-1G>A	NP_000368.1:n.778-1G>A
XM_011543977.1:c.778-1G>A	XP_011542279.1:n.778-1G>A
XM_011543977.2:c.778-1G>A	XP_011542279.1:n.778-1G>A
XM_017029786.1:c.778-1G>A	XP_016885275.1:n.778-1G>A
NM_000377.3:c.778-1G>A MANE Select	NP_000368.1:n.778-1G>A