Canonical Allele Identifier: CA2428354144

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48683822C= , CM000685.2:g.48683822C=	GRCh38
NC_000023.10:g.48542211C= , CM000685.1:g.48542211C=	GRCh37
NC_000023.9:g.48427155C=	NCBI36
NG_007877.1:g.5026C= , LRG_125:g.5026C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000483750.6:n.2C=
ENST00000698625.1:c.-32C=	ENSP00000513844.1:n.-32C=
ENST00000698635.1:c.-32C=	ENSP00000513850.1:n.-32C=
ENST00000376701.5:c.-32C= MANE Select	ENSP00000365891.4:n.-32C=
ENST00000376701.4:c.-32C=	ENSP00000365891.4:n.-32C=
ENST00000450772.5:c.-32C=	ENSP00000410537.1:n.-32C=
ENST00000465982.5:n.4C=
NM_000377.2:c.-32C= , LRG_125t1:c.-32C=	NP_000368.1:n.-32C=
XM_011543977.1:c.-32C=	XP_011542279.1:n.-32C=
XM_011543977.2:c.-32C=	XP_011542279.1:n.-32C=
XM_017029786.1:c.-32C=	XP_016885275.1:n.-32C=
NM_000377.3:c.-32C= MANE Select	NP_000368.1:n.-32C=