Canonical Allele Identifier: CA2693642833

Gene: WAS

Linked Data

• gnomAD v4: X-48683818-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48683818A>G , CM000685.2:g.48683818A>G	GRCh38
NC_000023.10:g.48542207A>G , CM000685.1:g.48542207A>G	GRCh37
NC_000023.9:g.48427151A>G	NCBI36
NG_007877.1:g.5022A>G , LRG_125:g.5022A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000698625.1:c.-34-2A>G	ENSP00000513844.1:n.-34-2A>G
ENST00000698635.1:c.-36A>G	ENSP00000513850.1:n.-36A>G
ENST00000376701.5:c.-36A>G MANE Select	ENSP00000365891.4:n.-36A>G
ENST00000376701.4:c.-36A>G	ENSP00000365891.4:n.-36A>G
ENST00000450772.5:c.-34-2A>G	ENSP00000410537.1:n.-34-2A>G
NM_000377.2:c.-36A>G , LRG_125t1:c.-36A>G	NP_000368.1:n.-36A>G
XM_011543977.1:c.-36A>G	XP_011542279.1:n.-36A>G
XM_011543977.2:c.-36A>G	XP_011542279.1:n.-36A>G
XM_017029786.1:c.-36A>G	XP_016885275.1:n.-36A>G
NM_000377.3:c.-36A>G MANE Select	NP_000368.1:n.-36A>G