Canonical Allele Identifier: CA412865459

Gene: WAS

Linked Data

• MyVariant Identifiers: chrX:g.48542304A>C (hg19) ; chrX:g.48683915A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48683915A>C , CM000685.2:g.48683915A>C	GRCh38
NC_000023.10:g.48542304A>C , CM000685.1:g.48542304A>C	GRCh37
NC_000023.9:g.48427248A>C	NCBI36
NG_007877.1:g.5119A>C , LRG_125:g.5119A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.95A>C
ENST00000698625.1:c.62A>C	ENSP00000513844.1:p.Asn21Thr
ENST00000698626.1:c.62A>C	ENSP00000513845.1:p.Asn21Thr
ENST00000698635.1:c.62A>C	ENSP00000513850.1:p.Asn21Thr
ENST00000376701.5:c.62A>C MANE Select	ENSP00000365891.4:p.Asn21Thr
ENST00000376701.4:c.62A>C	ENSP00000365891.4:p.Asn21Thr
ENST00000450772.5:c.62A>C	ENSP00000410537.1:p.Asn21Thr
ENST00000465982.5:n.97A>C
ENST00000483750.5:n.88A>C
NM_000377.2:c.62A>C , LRG_125t1:c.62A>C	NP_000368.1:p.Asn21Thr
XM_011543977.1:c.62A>C	XP_011542279.1:p.Asn21Thr
XM_011543977.2:c.62A>C	XP_011542279.1:p.Asn21Thr
XM_017029786.1:c.62A>C	XP_016885275.1:p.Asn21Thr
NM_000377.3:c.62A>C MANE Select	NP_000368.1:p.Asn21Thr