Canonical Allele Identifier: CA657966337
Gene: WAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48683791_48683792insA , CM000685.2:g.48683791_48683792insA GRCh38
NC_000023.10:g.48542180_48542181insA , CM000685.1:g.48542180_48542181insA GRCh37
NC_000023.9:g.48427124_48427125insA NCBI36
NG_007877.1:g.4995_4996insA , LRG_125:g.4995_4996insA

Transcript Alleles

HGVS Amino-acid change
ENST00000698625.1:c.-34-29_-34-28insA ENSP00000513844.1:n.-34-29_-34-28insA
ENST00000376701.4:c.-63_-62insA ENSP00000365891.4:n.-63_-62insA
ENST00000450772.5:c.-34-29_-34-28insA ENSP00000410537.1:n.-34-29_-34-28insA
XM_011543977.1:c.-63_-62insA XP_011542279.1:n.-63_-62insA
XM_011543977.2:c.-62-1_-62insA XP_011542279.1:n.-62-1_-62insA
XM_017029786.1:c.-63_-62insA XP_016885275.1:n.-63_-62insA