Canonical Allele Identifier: CA2428354137

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48683810C= , CM000685.2:g.48683810C=	GRCh38
NC_000023.10:g.48542199C= , CM000685.1:g.48542199C=	GRCh37
NC_000023.9:g.48427143C=	NCBI36
NG_007877.1:g.5014C= , LRG_125:g.5014C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000698625.1:c.-34-10C=	ENSP00000513844.1:n.-34-10C=
ENST00000698635.1:c.-44C=	ENSP00000513850.1:n.-44C=
ENST00000376701.5:c.-44C= MANE Select	ENSP00000365891.4:n.-44C=
ENST00000376701.4:c.-44C=	ENSP00000365891.4:n.-44C=
ENST00000450772.5:c.-34-10C=	ENSP00000410537.1:n.-34-10C=
NM_000377.2:c.-44C= , LRG_125t1:c.-44C=	NP_000368.1:n.-44C=
XM_011543977.1:c.-44C=	XP_011542279.1:n.-44C=
XM_011543977.2:c.-44C=	XP_011542279.1:n.-44C=
XM_017029786.1:c.-44C=	XP_016885275.1:n.-44C=
NM_000377.3:c.-44C= MANE Select	NP_000368.1:n.-44C=