Canonical Allele Identifier: CA516023607

Gene: WAS

Linked Data

• MyVariant Identifiers: chrX:g.48546482T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688093T>C , CM000685.2:g.48688093T>C	GRCh38
NC_000023.10:g.48546482T>C , CM000685.1:g.48546482T>C	GRCh37
NC_000023.9:g.48431426T>C	NCBI36
NG_007877.1:g.9297T>C , LRG_125:g.9297T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.807T>C
ENST00000490627.2:n.211T>C
ENST00000698625.1:c.774T>C	ENSP00000513844.1:p.Phe258=
ENST00000698626.1:c.774T>C	ENSP00000513845.1:p.Phe258=
ENST00000698635.1:c.774T>C	ENSP00000513850.1:p.Phe258=
ENST00000376701.5:c.774T>C MANE Select	ENSP00000365891.4:p.Phe258=
ENST00000376701.4:c.774T>C	ENSP00000365891.4:p.Phe258=
ENST00000465982.5:n.674T>C
ENST00000483750.5:n.800T>C
ENST00000490627.1:n.194T>C
NM_000377.2:c.774T>C , LRG_125t1:c.774T>C	NP_000368.1:p.Phe258=
XM_011543977.1:c.774T>C	XP_011542279.1:p.Phe258=
XM_011543977.2:c.774T>C	XP_011542279.1:p.Phe258=
XM_017029786.1:c.774T>C	XP_016885275.1:p.Phe258=
NM_000377.3:c.774T>C MANE Select	NP_000368.1:p.Phe258=