Canonical Allele Identifier: CA412866249

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48684322C>A , CM000685.2:g.48684322C>A	GRCh38
NC_000023.10:g.48542711C>A , CM000685.1:g.48542711C>A	GRCh37
NC_000023.9:g.48427655C>A	NCBI36
NG_007877.1:g.5526C>A , LRG_125:g.5526C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000377.3:c.172C>A MANE Select	NP_000368.1:p.Pro58Thr
ENST00000376701.5:c.172C>A MANE Select	ENSP00000365891.4:p.Pro58Thr
NM_000377.2:c.172C>A , LRG_125t1:c.172C>A	NP_000368.1:p.Pro58Thr
ENST00000376701.4:c.172C>A	ENSP00000365891.4:p.Pro58Thr
ENST00000450772.5:c.172C>A	ENSP00000410537.1:p.Pro58Thr
ENST00000465982.5:n.207C>A
ENST00000483750.5:n.198C>A
ENST00000483750.6:n.205C>A
ENST00000698625.1:c.172C>A	ENSP00000513844.1:p.Pro58Thr
ENST00000698626.1:c.172C>A	ENSP00000513845.1:p.Pro58Thr
ENST00000698635.1:c.172C>A	ENSP00000513850.1:p.Pro58Thr
XM_011543977.1:c.172C>A	XP_011542279.1:p.Pro58Thr
XM_011543977.2:c.172C>A	XP_011542279.1:p.Pro58Thr
XM_017029786.1:c.172C>A	XP_016885275.1:p.Pro58Thr