Canonical Allele Identifier: CA412873261

Gene: WAS

Linked Data

• MyVariant Identifiers: chrX:g.48547204G>T (hg19) ; chrX:g.48688815G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688815G>T , CM000685.2:g.48688815G>T	GRCh38
NC_000023.10:g.48547204G>T , CM000685.1:g.48547204G>T	GRCh37
NC_000023.9:g.48432148G>T	NCBI36
NG_007877.1:g.10019G>T , LRG_125:g.10019G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.331G>T
ENST00000698625.1:c.1087G>T	ENSP00000513844.1:p.Gly363Cys
ENST00000698626.1:c.1087G>T	ENSP00000513845.1:p.Gly363Cys
ENST00000698635.1:c.1087G>T	ENSP00000513850.1:p.Gly363Cys
ENST00000376701.5:c.1087G>T MANE Select	ENSP00000365891.4:p.Gly363Cys
ENST00000376701.4:c.1087G>T	ENSP00000365891.4:p.Gly363Cys
ENST00000474174.1:n.331G>T
NM_000377.2:c.1087G>T , LRG_125t1:c.1087G>T	NP_000368.1:p.Gly363Cys
XM_011543977.1:c.932-1G>T	XP_011542279.1:n.932-1G>T
XM_011543977.2:c.932-1G>T	XP_011542279.1:n.932-1G>T
XM_017029786.1:c.1087G>T	XP_016885275.1:p.Gly363Cys
NM_000377.3:c.1087G>T MANE Select	NP_000368.1:p.Gly363Cys