Canonical Allele Identifier: CA412872164

Gene: WAS

Linked Data

• MyVariant Identifiers: chrX:g.48546696A>T (hg19) ; chrX:g.48688307A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688307A>T , CM000685.2:g.48688307A>T	GRCh38
NC_000023.10:g.48546696A>T , CM000685.1:g.48546696A>T	GRCh37
NC_000023.9:g.48431640A>T	NCBI36
NG_007877.1:g.9511A>T , LRG_125:g.9511A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.29A>T
ENST00000483750.6:n.1021A>T
ENST00000698625.1:c.785A>T	ENSP00000513844.1:p.Asn262Ile
ENST00000698626.1:c.785A>T	ENSP00000513845.1:p.Asn262Ile
ENST00000698635.1:c.785A>T	ENSP00000513850.1:p.Asn262Ile
ENST00000376701.5:c.785A>T MANE Select	ENSP00000365891.4:p.Asn262Ile
ENST00000376701.4:c.785A>T	ENSP00000365891.4:p.Asn262Ile
ENST00000474174.1:n.29A>T
NM_000377.2:c.785A>T , LRG_125t1:c.785A>T	NP_000368.1:p.Asn262Ile
XM_011543977.1:c.785A>T	XP_011542279.1:p.Asn262Ile
XM_011543977.2:c.785A>T	XP_011542279.1:p.Asn262Ile
XM_017029786.1:c.785A>T	XP_016885275.1:p.Asn262Ile
NM_000377.3:c.785A>T MANE Select	NP_000368.1:p.Asn262Ile