Canonical Allele Identifier: CA2693643249

Gene: WAS

Linked Data

• gnomAD v4: X-48689192-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48689192T>C , CM000685.2:g.48689192T>C	GRCh38
NC_000023.10:g.48547581T>C , CM000685.1:g.48547581T>C	GRCh37
NC_000023.9:g.48432525T>C	NCBI36
NG_007877.1:g.10396T>C , LRG_125:g.10396T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.582+126T>C
ENST00000698625.1:c.1338+126T>C	ENSP00000513844.1:n.1338+126T>C
ENST00000698626.1:c.1338+126T>C	ENSP00000513845.1:n.1338+126T>C
ENST00000698635.1:c.1338+126T>C	ENSP00000513850.1:n.1338+126T>C
ENST00000376701.5:c.1338+126T>C MANE Select	ENSP00000365891.4:n.1338+126T>C
ENST00000376701.4:c.1338+126T>C	ENSP00000365891.4:n.1338+126T>C
ENST00000470107.1:n.47+126T>C
NM_000377.2:c.1338+126T>C , LRG_125t1:c.1338+126T>C	NP_000368.1:n.1338+126T>C
XM_011543977.1:c.1182+126T>C	XP_011542279.1:n.1182+126T>C
XM_011543977.2:c.1182+126T>C	XP_011542279.1:n.1182+126T>C
XM_017029786.1:c.1338+126T>C	XP_016885275.1:n.1338+126T>C
NM_000377.3:c.1338+126T>C MANE Select	NP_000368.1:n.1338+126T>C