Canonical Allele Identifier: CA412873751

Gene: WAS

Linked Data

• MyVariant Identifiers: chrX:g.48547452C>A (hg19) ; chrX:g.48689063C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48689063C>A , CM000685.2:g.48689063C>A	GRCh38
NC_000023.10:g.48547452C>A , CM000685.1:g.48547452C>A	GRCh37
NC_000023.9:g.48432396C>A	NCBI36
NG_007877.1:g.10267C>A , LRG_125:g.10267C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.579C>A
ENST00000698625.1:c.1335C>A	ENSP00000513844.1:p.Asn445Lys
ENST00000698626.1:c.1335C>A	ENSP00000513845.1:p.Asn445Lys
ENST00000698635.1:c.1335C>A	ENSP00000513850.1:p.Asn445Lys
ENST00000376701.5:c.1335C>A MANE Select	ENSP00000365891.4:p.Asn445Lys
ENST00000376701.4:c.1335C>A	ENSP00000365891.4:p.Asn445Lys
ENST00000470107.1:n.44C>A
NM_000377.2:c.1335C>A , LRG_125t1:c.1335C>A	NP_000368.1:p.Asn445Lys
XM_011543977.1:c.1179C>A	XP_011542279.1:p.Asn393Lys
XM_011543977.2:c.1179C>A	XP_011542279.1:p.Asn393Lys
XM_017029786.1:c.1335C>A	XP_016885275.1:p.Asn445Lys
NM_000377.3:c.1335C>A MANE Select	NP_000368.1:p.Asn445Lys