Canonical Allele Identifier: CA2428354143

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48683817C= , CM000685.2:g.48683817C=	GRCh38
NC_000023.10:g.48542206C= , CM000685.1:g.48542206C=	GRCh37
NC_000023.9:g.48427150C=	NCBI36
NG_007877.1:g.5021C= , LRG_125:g.5021C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000698625.1:c.-34-3C=	ENSP00000513844.1:n.-34-3C=
ENST00000698635.1:c.-37C=	ENSP00000513850.1:n.-37C=
ENST00000376701.5:c.-37C= MANE Select	ENSP00000365891.4:n.-37C=
ENST00000376701.4:c.-37C=	ENSP00000365891.4:n.-37C=
ENST00000450772.5:c.-34-3C=	ENSP00000410537.1:n.-34-3C=
NM_000377.2:c.-37C= , LRG_125t1:c.-37C=	NP_000368.1:n.-37C=
XM_011543977.1:c.-37C=	XP_011542279.1:n.-37C=
XM_011543977.2:c.-37C=	XP_011542279.1:n.-37C=
XM_017029786.1:c.-37C=	XP_016885275.1:n.-37C=
NM_000377.3:c.-37C= MANE Select	NP_000368.1:n.-37C=