Canonical Allele Identifier: CA2693643847

Gene: WAS

Linked Data

• gnomAD v4: X-48687935-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48687935C>T , CM000685.2:g.48687935C>T	GRCh38
NC_000023.10:g.48546324C>T , CM000685.1:g.48546324C>T	GRCh37
NC_000023.9:g.48431268C>T	NCBI36
NG_007877.1:g.9139C>T , LRG_125:g.9139C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000483750.6:n.768-119C>T
ENST00000490627.2:n.172-119C>T
ENST00000698625.1:c.735-119C>T	ENSP00000513844.1:n.735-119C>T
ENST00000698626.1:c.735-119C>T	ENSP00000513845.1:n.735-119C>T
ENST00000698635.1:c.735-119C>T	ENSP00000513850.1:n.735-119C>T
ENST00000376701.5:c.735-119C>T MANE Select	ENSP00000365891.4:n.735-119C>T
ENST00000376701.4:c.735-119C>T	ENSP00000365891.4:n.735-119C>T
ENST00000465982.5:n.635-119C>T
ENST00000483750.5:n.761-119C>T
ENST00000490627.1:n.155-119C>T
NM_000377.2:c.735-119C>T , LRG_125t1:c.735-119C>T	NP_000368.1:n.735-119C>T
XM_011543977.1:c.735-119C>T	XP_011542279.1:n.735-119C>T
XM_011543977.2:c.735-119C>T	XP_011542279.1:n.735-119C>T
XM_017029786.1:c.735-119C>T	XP_016885275.1:n.735-119C>T
NM_000377.3:c.735-119C>T MANE Select	NP_000368.1:n.735-119C>T