Canonical Allele Identifier: CA516356529

Gene: WAS

Linked Data

• gnomAD v4: X-48689058-C-T
• MyVariant Identifiers: chrX:g.48547447C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48689058C>T , CM000685.2:g.48689058C>T	GRCh38
NC_000023.10:g.48547447C>T , CM000685.1:g.48547447C>T	GRCh37
NC_000023.9:g.48432391C>T	NCBI36
NG_007877.1:g.10262C>T , LRG_125:g.10262C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.574C>T
ENST00000698625.1:c.1330C>T	ENSP00000513844.1:p.Leu444=
ENST00000698626.1:c.1330C>T	ENSP00000513845.1:p.Leu444=
ENST00000698635.1:c.1330C>T	ENSP00000513850.1:p.Leu444=
ENST00000376701.5:c.1330C>T MANE Select	ENSP00000365891.4:p.Leu444=
ENST00000376701.4:c.1330C>T	ENSP00000365891.4:p.Leu444=
ENST00000470107.1:n.39C>T
NM_000377.2:c.1330C>T , LRG_125t1:c.1330C>T	NP_000368.1:p.Leu444=
XM_011543977.1:c.1174C>T	XP_011542279.1:p.Leu392=
XM_011543977.2:c.1174C>T	XP_011542279.1:p.Leu392=
XM_017029786.1:c.1330C>T	XP_016885275.1:p.Leu444=
NM_000377.3:c.1330C>T MANE Select	NP_000368.1:p.Leu444=