Canonical Allele Identifier: CA412867479

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48685756T>C , CM000685.2:g.48685756T>C	GRCh38
NC_000023.10:g.48544145T>C , CM000685.1:g.48544145T>C	GRCh37
NC_000023.9:g.48429089T>C	NCBI36
NG_007877.1:g.6960T>C , LRG_125:g.6960T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000377.3:c.383T>C MANE Select	NP_000368.1:p.Phe128Ser
ENST00000376701.5:c.383T>C MANE Select	ENSP00000365891.4:p.Phe128Ser
NM_000377.2:c.383T>C , LRG_125t1:c.383T>C	NP_000368.1:p.Phe128Ser
ENST00000376701.4:c.383T>C	ENSP00000365891.4:p.Phe128Ser
ENST00000450772.5:c.383T>C	ENSP00000410537.1:p.Phe128Ser
ENST00000465982.5:n.418T>C
ENST00000483750.5:n.409T>C
ENST00000483750.6:n.416T>C
ENST00000698625.1:c.383T>C	ENSP00000513844.1:p.Phe128Ser
ENST00000698626.1:c.383T>C	ENSP00000513845.1:p.Phe128Ser
ENST00000698635.1:c.383T>C	ENSP00000513850.1:p.Phe128Ser
XM_011543977.1:c.383T>C	XP_011542279.1:p.Phe128Ser
XM_011543977.2:c.383T>C	XP_011542279.1:p.Phe128Ser
XM_017029786.1:c.383T>C	XP_016885275.1:p.Phe128Ser