Canonical Allele Identifier: CA2428355670

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688781_48688782delinsAC , CM000685.2:g.48688781_48688782delinsAC	GRCh38
NC_000023.10:g.48547170_48547171delinsAC , CM000685.1:g.48547170_48547171delinsAC	GRCh37
NC_000023.9:g.48432114_48432115delinsAC	NCBI36
NG_007877.1:g.9985_9986delinsAC , LRG_125:g.9985_9986delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.297_298delinsAC
ENST00000698625.1:c.1053_1054delinsAC	ENSP00000513844.1:p.Pro351=
ENST00000698626.1:c.1053_1054delinsAC	ENSP00000513845.1:p.Pro351=
ENST00000698635.1:c.1053_1054delinsAC	ENSP00000513850.1:p.Pro351=
ENST00000376701.5:c.1053_1054delinsAC MANE Select	ENSP00000365891.4:p.Pro351=
ENST00000376701.4:c.1053_1054delinsAC	ENSP00000365891.4:p.Pro351=
ENST00000474174.1:n.297_298delinsAC
NM_000377.2:c.1053_1054delinsAC , LRG_125t1:c.1053_1054delinsAC	NP_000368.1:p.Pro351=
XM_011543977.1:c.932-35_932-34delinsAC	XP_011542279.1:n.932-35_932-34delinsAC
XM_011543977.2:c.932-35_932-34delinsAC	XP_011542279.1:n.932-35_932-34delinsAC
XM_017029786.1:c.1053_1054delinsAC	XP_016885275.1:p.Pro351=
NM_000377.3:c.1053_1054delinsAC MANE Select	NP_000368.1:p.Pro351=