Canonical Allele Identifier: CA412873480

Gene: WAS

Linked Data

• ClinVar Variation Id: 658817
• ClinVar RCV Id: RCV000815707
• dbSNP Id: rs1602179582
• MyVariant Identifiers: chrX:g.48547313C>G (hg19) ; chrX:g.48688924C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688924C>G , CM000685.2:g.48688924C>G	GRCh38
NC_000023.10:g.48547313C>G , CM000685.1:g.48547313C>G	GRCh37
NC_000023.9:g.48432257C>G	NCBI36
NG_007877.1:g.10128C>G , LRG_125:g.10128C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.440C>G
ENST00000698625.1:c.1196C>G	ENSP00000513844.1:p.Pro399Arg
ENST00000698626.1:c.1196C>G	ENSP00000513845.1:p.Pro399Arg
ENST00000698635.1:c.1196C>G	ENSP00000513850.1:p.Pro399Arg
ENST00000376701.5:c.1196C>G MANE Select	ENSP00000365891.4:p.Pro399Arg
ENST00000376701.4:c.1196C>G	ENSP00000365891.4:p.Pro399Arg
ENST00000474174.1:n.440C>G
NM_000377.2:c.1196C>G , LRG_125t1:c.1196C>G	NP_000368.1:p.Pro399Arg
XM_011543977.1:c.1040C>G	XP_011542279.1:p.Pro347Arg
XM_011543977.2:c.1040C>G	XP_011542279.1:p.Pro347Arg
XM_017029786.1:c.1196C>G	XP_016885275.1:p.Pro399Arg
NM_000377.3:c.1196C>G MANE Select	NP_000368.1:p.Pro399Arg