Canonical Allele Identifier: CA412873267

Gene: WAS

Linked Data

• ClinVar Variation Id: 839782
• ClinVar RCV Id: RCV001041620 ; RCV001091017
• dbSNP Id: rs2062429013
• gnomAD v4: X-48688818-C-T
• MyVariant Identifiers: chrX:g.48547207C>T (hg19) ; chrX:g.48688818C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688818C>T , CM000685.2:g.48688818C>T	GRCh38
NC_000023.10:g.48547207C>T , CM000685.1:g.48547207C>T	GRCh37
NC_000023.9:g.48432151C>T	NCBI36
NG_007877.1:g.10022C>T , LRG_125:g.10022C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000474174.2:n.334C>T
ENST00000698625.1:c.1090C>T	ENSP00000513844.1:p.Arg364Ter
ENST00000698626.1:c.1090C>T	ENSP00000513845.1:p.Arg364Ter
ENST00000698635.1:c.1090C>T	ENSP00000513850.1:p.Arg364Ter
ENST00000376701.5:c.1090C>T MANE Select	ENSP00000365891.4:p.Arg364Ter
ENST00000376701.4:c.1090C>T	ENSP00000365891.4:p.Arg364Ter
ENST00000474174.1:n.334C>T
NM_000377.2:c.1090C>T , LRG_125t1:c.1090C>T	NP_000368.1:p.Arg364Ter
XM_011543977.1:c.934C>T	XP_011542279.1:p.Arg312Ter
XM_011543977.2:c.934C>T	XP_011542279.1:p.Arg312Ter
XM_017029786.1:c.1090C>T	XP_016885275.1:p.Arg364Ter
NM_000377.3:c.1090C>T MANE Select	NP_000368.1:p.Arg364Ter