Canonical Allele Identifier: CA2693645009

Gene: WAS

Linked Data

• gnomAD v4: X-48688931-A-ACCGCCG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688934_48688939dup , CM000685.2:g.48688934_48688939dup	GRCh38
NC_000023.10:g.48547323_48547328dup , CM000685.1:g.48547323_48547328dup	GRCh37
NC_000023.9:g.48432267_48432272dup	NCBI36
NG_007877.1:g.10138_10143dup , LRG_125:g.10138_10143dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.450_455dup
ENST00000698625.1:c.1206_1211dup	ENSP00000513844.1:p.Pro404_Ser405insProPro
ENST00000698626.1:c.1206_1211dup	ENSP00000513845.1:p.Pro404_Ser405insProPro
ENST00000698635.1:c.1206_1211dup	ENSP00000513850.1:p.Pro404_Ser405insProPro
ENST00000376701.5:c.1206_1211dup MANE Select	ENSP00000365891.4:p.Pro404_Ser405insProPro
ENST00000376701.4:c.1206_1211dup	ENSP00000365891.4:p.Pro404_Ser405insProPro
ENST00000474174.1:n.450_455dup
NM_000377.2:c.1206_1211dup , LRG_125t1:c.1206_1211dup	NP_000368.1:p.Pro404_Ser405insProPro
XM_011543977.1:c.1050_1055dup	XP_011542279.1:p.Pro352_Ser353insProPro
XM_011543977.2:c.1050_1055dup	XP_011542279.1:p.Pro352_Ser353insProPro
XM_017029786.1:c.1206_1211dup	XP_016885275.1:p.Pro404_Ser405insProPro
NM_000377.3:c.1206_1211dup MANE Select	NP_000368.1:p.Pro404_Ser405insProPro