Canonical Allele Identifier: CA2740092131

Gene: WAS

Linked Data

• ClinVar Variation Id: 2935869
• ClinVar RCV Id: RCV003793963

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688107T>A , CM000685.2:g.48688107T>A	GRCh38
NC_000023.10:g.48546496T>A , CM000685.1:g.48546496T>A	GRCh37
NC_000023.9:g.48431440T>A	NCBI36
NG_007877.1:g.9311T>A , LRG_125:g.9311T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000483750.6:n.821T>A
ENST00000490627.2:n.225T>A
ENST00000698625.1:c.777+11T>A	ENSP00000513844.1:n.777+11T>A
ENST00000698626.1:c.777+11T>A	ENSP00000513845.1:n.777+11T>A
ENST00000698635.1:c.777+11T>A	ENSP00000513850.1:n.777+11T>A
ENST00000376701.5:c.777+11T>A MANE Select	ENSP00000365891.4:n.777+11T>A
ENST00000376701.4:c.777+11T>A	ENSP00000365891.4:n.777+11T>A
ENST00000465982.5:n.688T>A
ENST00000483750.5:n.814T>A
ENST00000490627.1:n.208T>A
NM_000377.2:c.777+11T>A , LRG_125t1:c.777+11T>A	NP_000368.1:n.777+11T>A
XM_011543977.1:c.777+11T>A	XP_011542279.1:n.777+11T>A
XM_011543977.2:c.777+11T>A	XP_011542279.1:n.777+11T>A
XM_017029786.1:c.777+11T>A	XP_016885275.1:n.777+11T>A
NM_000377.3:c.777+11T>A MANE Select	NP_000368.1:n.777+11T>A