Canonical Allele Identifier: CA2820814514

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48683812G>A , CM000685.2:g.48683812G>A	GRCh38
NC_000023.10:g.48542201G>A , CM000685.1:g.48542201G>A	GRCh37
NC_000023.9:g.48427145G>A	NCBI36
NG_007877.1:g.5016G>A , LRG_125:g.5016G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698625.1:c.-34-8G>A	ENSP00000513844.1:n.-34-8G>A
ENST00000698635.1:c.-42G>A	ENSP00000513850.1:n.-42G>A
ENST00000376701.5:c.-42G>A MANE Select	ENSP00000365891.4:n.-42G>A
ENST00000376701.4:c.-42G>A	ENSP00000365891.4:n.-42G>A
ENST00000450772.5:c.-34-8G>A	ENSP00000410537.1:n.-34-8G>A
NM_000377.2:c.-42G>A , LRG_125t1:c.-42G>A	NP_000368.1:n.-42G>A
XM_011543977.1:c.-42G>A	XP_011542279.1:n.-42G>A
XM_011543977.2:c.-42G>A	XP_011542279.1:n.-42G>A
XM_017029786.1:c.-42G>A	XP_016885275.1:n.-42G>A
NM_000377.3:c.-42G>A MANE Select	NP_000368.1:n.-42G>A