Canonical Allele Identifier: CA2579600563

Gene: WAS

Linked Data

• gnomAD v4: X-48683825-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48683825C>T , CM000685.2:g.48683825C>T	GRCh38
NC_000023.10:g.48542214C>T , CM000685.1:g.48542214C>T	GRCh37
NC_000023.9:g.48427158C>T	NCBI36
NG_007877.1:g.5029C>T , LRG_125:g.5029C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000483750.6:n.5C>T
ENST00000698625.1:c.-29C>T	ENSP00000513844.1:n.-29C>T
ENST00000698635.1:c.-29C>T	ENSP00000513850.1:n.-29C>T
ENST00000376701.5:c.-29C>T MANE Select	ENSP00000365891.4:n.-29C>T
ENST00000376701.4:c.-29C>T	ENSP00000365891.4:n.-29C>T
ENST00000450772.5:c.-29C>T	ENSP00000410537.1:n.-29C>T
ENST00000465982.5:n.7C>T
NM_000377.2:c.-29C>T , LRG_125t1:c.-29C>T	NP_000368.1:n.-29C>T
XM_011543977.1:c.-29C>T	XP_011542279.1:n.-29C>T
XM_011543977.2:c.-29C>T	XP_011542279.1:n.-29C>T
XM_017029786.1:c.-29C>T	XP_016885275.1:n.-29C>T
NM_000377.3:c.-29C>T MANE Select	NP_000368.1:n.-29C>T