Canonical Allele Identifier: CA412865211

Gene: WAS

Linked Data

• MyVariant Identifiers: chrX:g.48542268G>T (hg19) ; chrX:g.48683879G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48683879G>T , CM000685.2:g.48683879G>T	GRCh38
NC_000023.10:g.48542268G>T , CM000685.1:g.48542268G>T	GRCh37
NC_000023.9:g.48427212G>T	NCBI36
NG_007877.1:g.5083G>T , LRG_125:g.5083G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.59G>T
ENST00000698625.1:c.26G>T	ENSP00000513844.1:p.Arg9Met
ENST00000698626.1:c.26G>T	ENSP00000513845.1:p.Arg9Met
ENST00000698635.1:c.26G>T	ENSP00000513850.1:p.Arg9Met
ENST00000376701.5:c.26G>T MANE Select	ENSP00000365891.4:p.Arg9Met
ENST00000376701.4:c.26G>T	ENSP00000365891.4:p.Arg9Met
ENST00000450772.5:c.26G>T	ENSP00000410537.1:p.Arg9Met
ENST00000465982.5:n.61G>T
ENST00000483750.5:n.52G>T
NM_000377.2:c.26G>T , LRG_125t1:c.26G>T	NP_000368.1:p.Arg9Met
XM_011543977.1:c.26G>T	XP_011542279.1:p.Arg9Met
XM_011543977.2:c.26G>T	XP_011542279.1:p.Arg9Met
XM_017029786.1:c.26G>T	XP_016885275.1:p.Arg9Met
NM_000377.3:c.26G>T MANE Select	NP_000368.1:p.Arg9Met