Canonical Allele Identifier: CA2579600672

Gene: WAS

Linked Data

• ClinVar Variation Id: 2928021
• ClinVar RCV Id: RCV003786843

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688038_48688039insGT , CM000685.2:g.48688038_48688039insGT	GRCh38
NC_000023.10:g.48546427_48546428insGT , CM000685.1:g.48546427_48546428insGT	GRCh37
NC_000023.9:g.48431371_48431372insGT	NCBI36
NG_007877.1:g.9242_9243insGT , LRG_125:g.9242_9243insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.768-16_768-15insGT
ENST00000490627.2:n.172-16_172-15insGT
ENST00000698625.1:c.735-16_735-15insGT	ENSP00000513844.1:n.735-16_735-15insGT
ENST00000698626.1:c.735-16_735-15insGT	ENSP00000513845.1:n.735-16_735-15insGT
ENST00000698635.1:c.735-16_735-15insGT	ENSP00000513850.1:n.735-16_735-15insGT
ENST00000376701.5:c.735-16_735-15insGT MANE Select	ENSP00000365891.4:n.735-16_735-15insGT
ENST00000376701.4:c.735-16_735-15insGT	ENSP00000365891.4:n.735-16_735-15insGT
ENST00000465982.5:n.635-16_635-15insGT
ENST00000483750.5:n.761-16_761-15insGT
ENST00000490627.1:n.155-16_155-15insGT
NM_000377.2:c.735-16_735-15insGT , LRG_125t1:c.735-16_735-15insGT	NP_000368.1:n.735-16_735-15insGT
XM_011543977.1:c.735-16_735-15insGT	XP_011542279.1:n.735-16_735-15insGT
XM_011543977.2:c.735-16_735-15insGT	XP_011542279.1:n.735-16_735-15insGT
XM_017029786.1:c.735-16_735-15insGT	XP_016885275.1:n.735-16_735-15insGT
NM_000377.3:c.735-16_735-15insGT MANE Select	NP_000368.1:n.735-16_735-15insGT