Canonical Allele Identifier: CA2693643822

Gene: WAS

Linked Data

• gnomAD v4: X-48687903-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48687903C>G , CM000685.2:g.48687903C>G	GRCh38
NC_000023.10:g.48546292C>G , CM000685.1:g.48546292C>G	GRCh37
NC_000023.9:g.48431236C>G	NCBI36
NG_007877.1:g.9107C>G , LRG_125:g.9107C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000483750.6:n.768-151C>G
ENST00000490627.2:n.172-151C>G
ENST00000698625.1:c.735-151C>G	ENSP00000513844.1:n.735-151C>G
ENST00000698626.1:c.735-151C>G	ENSP00000513845.1:n.735-151C>G
ENST00000698635.1:c.735-151C>G	ENSP00000513850.1:n.735-151C>G
ENST00000376701.5:c.735-151C>G MANE Select	ENSP00000365891.4:n.735-151C>G
ENST00000376701.4:c.735-151C>G	ENSP00000365891.4:n.735-151C>G
ENST00000465982.5:n.635-151C>G
ENST00000483750.5:n.761-151C>G
ENST00000490627.1:n.155-151C>G
NM_000377.2:c.735-151C>G , LRG_125t1:c.735-151C>G	NP_000368.1:n.735-151C>G
XM_011543977.1:c.735-151C>G	XP_011542279.1:n.735-151C>G
XM_011543977.2:c.735-151C>G	XP_011542279.1:n.735-151C>G
XM_017029786.1:c.735-151C>G	XP_016885275.1:n.735-151C>G
NM_000377.3:c.735-151C>G MANE Select	NP_000368.1:n.735-151C>G