Canonical Allele Identifier: CA10404056

Gene: WAS

Linked Data

• dbSNP Id: rs782347339
• ExAC: X:48547344 A / C
• gnomAD v4: X-48688955-A-C
• MyVariant Identifiers: chrX:g.48547344A>C (hg19) ; chrX:g.48688955A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688955A>C , CM000685.2:g.48688955A>C	GRCh38
NC_000023.10:g.48547344A>C , CM000685.1:g.48547344A>C	GRCh37
NC_000023.9:g.48432288A>C	NCBI36
NG_007877.1:g.10159A>C , LRG_125:g.10159A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.471A>C
ENST00000698625.1:c.1227A>C	ENSP00000513844.1:p.Gly409=
ENST00000698626.1:c.1227A>C	ENSP00000513845.1:p.Gly409=
ENST00000698635.1:c.1227A>C	ENSP00000513850.1:p.Gly409=
ENST00000376701.5:c.1227A>C MANE Select	ENSP00000365891.4:p.Gly409=
ENST00000376701.4:c.1227A>C	ENSP00000365891.4:p.Gly409=
ENST00000474174.1:n.471A>C
NM_000377.2:c.1227A>C , LRG_125t1:c.1227A>C	NP_000368.1:p.Gly409=
XM_011543977.1:c.1071A>C	XP_011542279.1:p.Gly357=
XM_011543977.2:c.1071A>C	XP_011542279.1:p.Gly357=
XM_017029786.1:c.1227A>C	XP_016885275.1:p.Gly409=
NM_000377.3:c.1227A>C MANE Select	NP_000368.1:p.Gly409=