Canonical Allele Identifier: CA412874033

Gene: WAS

Linked Data

• ClinVar Variation Id: 1074601
• ClinVar RCV Id: RCV001387958
• dbSNP Id: rs2147267350
• MyVariant Identifiers: chrX:g.48547825T>G (hg19) ; chrX:g.48689436T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48689436T>G , CM000685.2:g.48689436T>G	GRCh38
NC_000023.10:g.48547825T>G , CM000685.1:g.48547825T>G	GRCh37
NC_000023.9:g.48432769T>G	NCBI36
NG_007877.1:g.10640T>G , LRG_125:g.10640T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000698625.1:c.1453+2T>G	ENSP00000513844.1:n.1453+2T>G
ENST00000698626.1:c.1453+2T>G	ENSP00000513845.1:n.1453+2T>G
ENST00000698635.1:c.1453+2T>G	ENSP00000513850.1:n.1453+2T>G
ENST00000376701.5:c.1453+2T>G MANE Select	ENSP00000365891.4:n.1453+2T>G
ENST00000376701.4:c.1453+2T>G	ENSP00000365891.4:n.1453+2T>G
ENST00000470107.1:n.164T>G
NM_000377.2:c.1453+2T>G , LRG_125t1:c.1453+2T>G	NP_000368.1:n.1453+2T>G
XM_011543977.1:c.1297+2T>G	XP_011542279.1:n.1297+2T>G
XM_011543977.2:c.1297+2T>G	XP_011542279.1:n.1297+2T>G
XM_017029786.1:c.1453+2T>G	XP_016885275.1:n.1453+2T>G
NM_000377.3:c.1453+2T>G MANE Select	NP_000368.1:n.1453+2T>G