Canonical Allele Identifier: CA2428354132
Gene: WAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48683791G= , CM000685.2:g.48683791G= GRCh38
NC_000023.10:g.48542180G= , CM000685.1:g.48542180G= GRCh37
NC_000023.9:g.48427124G= NCBI36
NG_007877.1:g.4995G= , LRG_125:g.4995G=

Transcript Alleles

HGVS Amino-acid change
ENST00000698625.1:c.-34-29G= ENSP00000513844.1:n.-34-29G=
ENST00000376701.4:c.-63G= ENSP00000365891.4:n.-63G=
ENST00000450772.5:c.-34-29G= ENSP00000410537.1:n.-34-29G=
XM_011543977.1:c.-63G= XP_011542279.1:n.-63G=
XM_017029786.1:c.-63G= XP_016885275.1:n.-63G=