Canonical Allele Identifier: CA2428355613

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688638_48688640delinsATG , CM000685.2:g.48688638_48688640delinsATG	GRCh38
NC_000023.10:g.48547027_48547029delinsATG , CM000685.1:g.48547027_48547029delinsATG	GRCh37
NC_000023.9:g.48431971_48431973delinsATG	NCBI36
NG_007877.1:g.9842_9844delinsATG , LRG_125:g.9842_9844delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.176-22_176-20delinsATG
ENST00000698625.1:c.932-22_932-20delinsATG	ENSP00000513844.1:n.932-22_932-20delinsATG
ENST00000698626.1:c.932-22_932-20delinsATG	ENSP00000513845.1:n.932-22_932-20delinsATG
ENST00000698635.1:c.932-22_932-20delinsATG	ENSP00000513850.1:n.932-22_932-20delinsATG
ENST00000376701.5:c.932-22_932-20delinsATG MANE Select	ENSP00000365891.4:n.932-22_932-20delinsATG
ENST00000376701.4:c.932-22_932-20delinsATG	ENSP00000365891.4:n.932-22_932-20delinsATG
ENST00000474174.1:n.176-22_176-20delinsATG
NM_000377.2:c.932-22_932-20delinsATG , LRG_125t1:c.932-22_932-20delinsATG	NP_000368.1:n.932-22_932-20delinsATG
XM_011543977.1:c.932-178_932-176delinsATG	XP_011542279.1:n.932-178_932-176delinsATG
XM_011543977.2:c.932-178_932-176delinsATG	XP_011542279.1:n.932-178_932-176delinsATG
XM_017029786.1:c.932-22_932-20delinsATG	XP_016885275.1:n.932-22_932-20delinsATG
NM_000377.3:c.932-22_932-20delinsATG MANE Select	NP_000368.1:n.932-22_932-20delinsATG