Canonical Allele Identifier: CA2428355654

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688723_48688724delinsTG , CM000685.2:g.48688723_48688724delinsTG	GRCh38
NC_000023.10:g.48547112_48547113delinsTG , CM000685.1:g.48547112_48547113delinsTG	GRCh37
NC_000023.9:g.48432056_48432057delinsTG	NCBI36
NG_007877.1:g.9927_9928delinsTG , LRG_125:g.9927_9928delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474174.2:n.239_240delinsTG
ENST00000698625.1:c.995_996delinsTG	ENSP00000513844.1:p.Val332=
ENST00000698626.1:c.995_996delinsTG	ENSP00000513845.1:p.Val332=
ENST00000698635.1:c.995_996delinsTG	ENSP00000513850.1:p.Val332=
ENST00000376701.5:c.995_996delinsTG MANE Select	ENSP00000365891.4:p.Val332=
ENST00000376701.4:c.995_996delinsTG	ENSP00000365891.4:p.Val332=
ENST00000474174.1:n.239_240delinsTG
NM_000377.2:c.995_996delinsTG , LRG_125t1:c.995_996delinsTG	NP_000368.1:p.Val332=
XM_011543977.1:c.932-93_932-92delinsTG	XP_011542279.1:n.932-93_932-92delinsTG
XM_011543977.2:c.932-93_932-92delinsTG	XP_011542279.1:n.932-93_932-92delinsTG
XM_017029786.1:c.995_996delinsTG	XP_016885275.1:p.Val332=
NM_000377.3:c.995_996delinsTG MANE Select	NP_000368.1:p.Val332=