Canonical Allele Identifier: CA412873634

Gene: WAS

Linked Data

• MyVariant Identifiers: chrX:g.48547396C>A (hg19) ; chrX:g.48689007C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48689007C>A , CM000685.2:g.48689007C>A	GRCh38
NC_000023.10:g.48547396C>A , CM000685.1:g.48547396C>A	GRCh37
NC_000023.9:g.48432340C>A	NCBI36
NG_007877.1:g.10211C>A , LRG_125:g.10211C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.523C>A
ENST00000698625.1:c.1279C>A	ENSP00000513844.1:p.Pro427Thr
ENST00000698626.1:c.1279C>A	ENSP00000513845.1:p.Pro427Thr
ENST00000698635.1:c.1279C>A	ENSP00000513850.1:p.Pro427Thr
ENST00000376701.5:c.1279C>A MANE Select	ENSP00000365891.4:p.Pro427Thr
ENST00000376701.4:c.1279C>A	ENSP00000365891.4:p.Pro427Thr
NM_000377.2:c.1279C>A , LRG_125t1:c.1279C>A	NP_000368.1:p.Pro427Thr
XM_011543977.1:c.1123C>A	XP_011542279.1:p.Pro375Thr
XM_011543977.2:c.1123C>A	XP_011542279.1:p.Pro375Thr
XM_017029786.1:c.1279C>A	XP_016885275.1:p.Pro427Thr
NM_000377.3:c.1279C>A MANE Select	NP_000368.1:p.Pro427Thr