Canonical Allele Identifier: CA412872209

Gene: WAS

Linked Data

• MyVariant Identifiers: chrX:g.48546717G>C (hg19) ; chrX:g.48688328G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688328G>C , CM000685.2:g.48688328G>C	GRCh38
NC_000023.10:g.48546717G>C , CM000685.1:g.48546717G>C	GRCh37
NC_000023.9:g.48431661G>C	NCBI36
NG_007877.1:g.9532G>C , LRG_125:g.9532G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.50G>C
ENST00000483750.6:n.1042G>C
ENST00000698625.1:c.806G>C	ENSP00000513844.1:p.Ser269Thr
ENST00000698626.1:c.806G>C	ENSP00000513845.1:p.Ser269Thr
ENST00000698635.1:c.806G>C	ENSP00000513850.1:p.Ser269Thr
ENST00000376701.5:c.806G>C MANE Select	ENSP00000365891.4:p.Ser269Thr
ENST00000376701.4:c.806G>C	ENSP00000365891.4:p.Ser269Thr
ENST00000474174.1:n.50G>C
NM_000377.2:c.806G>C , LRG_125t1:c.806G>C	NP_000368.1:p.Ser269Thr
XM_011543977.1:c.806G>C	XP_011542279.1:p.Ser269Thr
XM_011543977.2:c.806G>C	XP_011542279.1:p.Ser269Thr
XM_017029786.1:c.806G>C	XP_016885275.1:p.Ser269Thr
NM_000377.3:c.806G>C MANE Select	NP_000368.1:p.Ser269Thr