Canonical Allele Identifier: CA2428355693

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688820_48688821delinsAG , CM000685.2:g.48688820_48688821delinsAG	GRCh38
NC_000023.10:g.48547209_48547210delinsAG , CM000685.1:g.48547209_48547210delinsAG	GRCh37
NC_000023.9:g.48432153_48432154delinsAG	NCBI36
NG_007877.1:g.10024_10025delinsAG , LRG_125:g.10024_10025delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.336_337delinsAG
ENST00000698625.1:c.1092_1093delinsAG	ENSP00000513844.1:p.Arg364=
ENST00000698626.1:c.1092_1093delinsAG	ENSP00000513845.1:p.Arg364=
ENST00000698635.1:c.1092_1093delinsAG	ENSP00000513850.1:p.Arg364=
ENST00000376701.5:c.1092_1093delinsAG MANE Select	ENSP00000365891.4:p.Arg364=
ENST00000376701.4:c.1092_1093delinsAG	ENSP00000365891.4:p.Arg364=
ENST00000474174.1:n.336_337delinsAG
NM_000377.2:c.1092_1093delinsAG , LRG_125t1:c.1092_1093delinsAG	NP_000368.1:p.Arg364=
XM_011543977.1:c.936_937delinsAG	XP_011542279.1:p.Arg312=
XM_011543977.2:c.936_937delinsAG	XP_011542279.1:p.Arg312=
XM_017029786.1:c.1092_1093delinsAG	XP_016885275.1:p.Arg364=
NM_000377.3:c.1092_1093delinsAG MANE Select	NP_000368.1:p.Arg364=