Canonical Allele Identifier: CA641901819

Gene: WAS

Linked Data

• dbSNP Id: rs1557006983
• gnomAD v2: X-48546566-G-C
• gnomAD v3: X-48688177-G-C
• gnomAD v4: X-48688177-G-C
• MyVariant Identifiers: chrX:g.48546566G>C (hg19) ; chrX:g.48688177G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688177G>C , CM000685.2:g.48688177G>C	GRCh38
NC_000023.10:g.48546566G>C , CM000685.1:g.48546566G>C	GRCh37
NC_000023.9:g.48431510G>C	NCBI36
NG_007877.1:g.9381G>C , LRG_125:g.9381G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.891G>C
ENST00000698625.1:c.777+81G>C	ENSP00000513844.1:n.777+81G>C
ENST00000698626.1:c.777+81G>C	ENSP00000513845.1:n.777+81G>C
ENST00000698635.1:c.777+81G>C	ENSP00000513850.1:n.777+81G>C
ENST00000376701.5:c.777+81G>C MANE Select	ENSP00000365891.4:n.777+81G>C
ENST00000376701.4:c.777+81G>C	ENSP00000365891.4:n.777+81G>C
ENST00000483750.5:n.884G>C
NM_000377.2:c.777+81G>C , LRG_125t1:c.777+81G>C	NP_000368.1:n.777+81G>C
XM_011543977.1:c.777+81G>C	XP_011542279.1:n.777+81G>C
XM_011543977.2:c.777+81G>C	XP_011542279.1:n.777+81G>C
XM_017029786.1:c.777+81G>C	XP_016885275.1:n.777+81G>C
NM_000377.3:c.777+81G>C MANE Select	NP_000368.1:n.777+81G>C