Canonical Allele Identifier: CA412872565

Gene: WAS

Linked Data

• ClinVar Variation Id: 998525
• ClinVar RCV Id: RCV001294393
• dbSNP Id: rs1215457658
• COSMIC: COSM4740743
• MyVariant Identifiers: chrX:g.48546836C>T (hg19) ; chrX:g.48688447C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688447C>T , CM000685.2:g.48688447C>T	GRCh38
NC_000023.10:g.48546836C>T , CM000685.1:g.48546836C>T	GRCh37
NC_000023.9:g.48431780C>T	NCBI36
NG_007877.1:g.9651C>T , LRG_125:g.9651C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.169C>T
ENST00000698625.1:c.925C>T	ENSP00000513844.1:p.Arg309Cys
ENST00000698626.1:c.925C>T	ENSP00000513845.1:p.Arg309Cys
ENST00000698635.1:c.925C>T	ENSP00000513850.1:p.Arg309Cys
ENST00000376701.5:c.925C>T MANE Select	ENSP00000365891.4:p.Arg309Cys
ENST00000376701.4:c.925C>T	ENSP00000365891.4:p.Arg309Cys
ENST00000474174.1:n.169C>T
NM_000377.2:c.925C>T , LRG_125t1:c.925C>T	NP_000368.1:p.Arg309Cys
XM_011543977.1:c.925C>T	XP_011542279.1:p.Arg309Cys
XM_011543977.2:c.925C>T	XP_011542279.1:p.Arg309Cys
XM_017029786.1:c.925C>T	XP_016885275.1:p.Arg309Cys
NM_000377.3:c.925C>T MANE Select	NP_000368.1:p.Arg309Cys