Canonical Allele Identifier: CA412866685

Gene: WAS

Linked Data

• ClinVar Variation Id: 528221
• ClinVar RCV Id: RCV000633306
• dbSNP Id: rs1557006354
• MyVariant Identifiers: chrX:g.48542810C>T (hg19) ; chrX:g.48684421C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48684421C>T , CM000685.2:g.48684421C>T	GRCh38
NC_000023.10:g.48542810C>T , CM000685.1:g.48542810C>T	GRCh37
NC_000023.9:g.48427754C>T	NCBI36
NG_007877.1:g.5625C>T , LRG_125:g.5625C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.304C>T
ENST00000698625.1:c.271C>T	ENSP00000513844.1:p.Gln91Ter
ENST00000698626.1:c.271C>T	ENSP00000513845.1:p.Gln91Ter
ENST00000698635.1:c.271C>T	ENSP00000513850.1:p.Gln91Ter
ENST00000376701.5:c.271C>T MANE Select	ENSP00000365891.4:p.Gln91Ter
ENST00000376701.4:c.271C>T	ENSP00000365891.4:p.Gln91Ter
ENST00000450772.5:c.271C>T	ENSP00000410537.1:p.Gln91Ter
ENST00000465982.5:n.306C>T
ENST00000483750.5:n.297C>T
NM_000377.2:c.271C>T , LRG_125t1:c.271C>T	NP_000368.1:p.Gln91Ter
XM_011543977.1:c.271C>T	XP_011542279.1:p.Gln91Ter
XM_011543977.2:c.271C>T	XP_011542279.1:p.Gln91Ter
XM_017029786.1:c.271C>T	XP_016885275.1:p.Gln91Ter
NM_000377.3:c.271C>T MANE Select	NP_000368.1:p.Gln91Ter