Canonical Allele Identifier: CA516355806

Gene: WAS

Linked Data

• MyVariant Identifiers: chrX:g.48543938T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48685549T>A , CM000685.2:g.48685549T>A	GRCh38
NC_000023.10:g.48543938T>A , CM000685.1:g.48543938T>A	GRCh37
NC_000023.9:g.48428882T>A	NCBI36
NG_007877.1:g.6753T>A , LRG_125:g.6753T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.309T>A
ENST00000698625.1:c.276T>A	ENSP00000513844.1:p.Ala92=
ENST00000698626.1:c.276T>A	ENSP00000513845.1:p.Ala92=
ENST00000698635.1:c.276T>A	ENSP00000513850.1:p.Ala92=
ENST00000376701.5:c.276T>A MANE Select	ENSP00000365891.4:p.Ala92=
ENST00000376701.4:c.276T>A	ENSP00000365891.4:p.Ala92=
ENST00000450772.5:c.276T>A	ENSP00000410537.1:p.Ala92=
ENST00000465982.5:n.311T>A
ENST00000483750.5:n.302T>A
NM_000377.2:c.276T>A , LRG_125t1:c.276T>A	NP_000368.1:p.Ala92=
XM_011543977.1:c.276T>A	XP_011542279.1:p.Ala92=
XM_011543977.2:c.276T>A	XP_011542279.1:p.Ala92=
XM_017029786.1:c.276T>A	XP_016885275.1:p.Ala92=
NM_000377.3:c.276T>A MANE Select	NP_000368.1:p.Ala92=