Canonical Allele Identifier: CA2739289592

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48685547_48685549delinsAAG , CM000685.2:g.48685547_48685549delinsAAG	GRCh38
NC_000023.10:g.48543936_48543938delinsAAG , CM000685.1:g.48543936_48543938delinsAAG	GRCh37
NC_000023.9:g.48428880_48428882delinsAAG	NCBI36
NG_007877.1:g.6751_6753delinsAAG , LRG_125:g.6751_6753delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.307_309delinsAAG
ENST00000698625.1:c.274_276delinsAAG	ENSP00000513844.1:p.Ala92Lys
ENST00000698626.1:c.274_276delinsAAG	ENSP00000513845.1:p.Ala92Lys
ENST00000698635.1:c.274_276delinsAAG	ENSP00000513850.1:p.Ala92Lys
ENST00000376701.5:c.274_276delinsAAG MANE Select	ENSP00000365891.4:p.Ala92Lys
ENST00000376701.4:c.274_276delinsAAG	ENSP00000365891.4:p.Ala92Lys
ENST00000450772.5:c.274_276delinsAAG	ENSP00000410537.1:p.Ala92Lys
ENST00000465982.5:n.309_311delinsAAG
ENST00000483750.5:n.300_302delinsAAG
NM_000377.2:c.274_276delinsAAG , LRG_125t1:c.274_276delinsAAG	NP_000368.1:p.Ala92Lys
XM_011543977.1:c.274_276delinsAAG	XP_011542279.1:p.Ala92Lys
XM_011543977.2:c.274_276delinsAAG	XP_011542279.1:p.Ala92Lys
XM_017029786.1:c.274_276delinsAAG	XP_016885275.1:p.Ala92Lys
NM_000377.3:c.274_276delinsAAG MANE Select	NP_000368.1:p.Ala92Lys