Canonical Allele Identifier: CA2579600562

Gene: WAS

Linked Data

• gnomAD v4: X-48683809-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48683809C>A , CM000685.2:g.48683809C>A	GRCh38
NC_000023.10:g.48542198C>A , CM000685.1:g.48542198C>A	GRCh37
NC_000023.9:g.48427142C>A	NCBI36
NG_007877.1:g.5013C>A , LRG_125:g.5013C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698625.1:c.-34-11C>A	ENSP00000513844.1:n.-34-11C>A
ENST00000698635.1:c.-45C>A	ENSP00000513850.1:n.-45C>A
ENST00000376701.5:c.-45C>A MANE Select	ENSP00000365891.4:n.-45C>A
ENST00000376701.4:c.-45C>A	ENSP00000365891.4:n.-45C>A
ENST00000450772.5:c.-34-11C>A	ENSP00000410537.1:n.-34-11C>A
NM_000377.2:c.-45C>A , LRG_125t1:c.-45C>A	NP_000368.1:n.-45C>A
XM_011543977.1:c.-45C>A	XP_011542279.1:n.-45C>A
XM_011543977.2:c.-45C>A	XP_011542279.1:n.-45C>A
XM_017029786.1:c.-45C>A	XP_016885275.1:n.-45C>A
NM_000377.3:c.-45C>A MANE Select	NP_000368.1:n.-45C>A