Canonical Allele Identifier: CA2428355787

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48689000_48689005delinsCCTGGC , CM000685.2:g.48689000_48689005delinsCCTGGC	GRCh38
NC_000023.10:g.48547389_48547394delinsCCTGGC , CM000685.1:g.48547389_48547394delinsCCTGGC	GRCh37
NC_000023.9:g.48432333_48432338delinsCCTGGC	NCBI36
NG_007877.1:g.10204_10209delinsCCTGGC , LRG_125:g.10204_10209delinsCCTGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.516_521delinsCCTGGC
ENST00000698625.1:c.1272_1277delinsCCTGGC	ENSP00000513844.1:p.Gly424=
ENST00000698626.1:c.1272_1277delinsCCTGGC	ENSP00000513845.1:p.Gly424=
ENST00000698635.1:c.1272_1277delinsCCTGGC	ENSP00000513850.1:p.Gly424=
ENST00000376701.5:c.1272_1277delinsCCTGGC MANE Select	ENSP00000365891.4:p.Gly424=
ENST00000376701.4:c.1272_1277delinsCCTGGC	ENSP00000365891.4:p.Gly424=
NM_000377.2:c.1272_1277delinsCCTGGC , LRG_125t1:c.1272_1277delinsCCTGGC	NP_000368.1:p.Gly424=
XM_011543977.1:c.1116_1121delinsCCTGGC	XP_011542279.1:p.Gly372=
XM_011543977.2:c.1116_1121delinsCCTGGC	XP_011542279.1:p.Gly372=
XM_017029786.1:c.1272_1277delinsCCTGGC	XP_016885275.1:p.Gly424=
NM_000377.3:c.1272_1277delinsCCTGGC MANE Select	NP_000368.1:p.Gly424=