Canonical Allele Identifier: CA2820814515
Gene: WAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48683821G>C , CM000685.2:g.48683821G>C GRCh38
NC_000023.10:g.48542210G>C , CM000685.1:g.48542210G>C GRCh37
NC_000023.9:g.48427154G>C NCBI36
NG_007877.1:g.5025G>C , LRG_125:g.5025G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000483750.6:n.1G>C
ENST00000698625.1:c.-33G>C ENSP00000513844.1:n.-33G>C
ENST00000698635.1:c.-33G>C ENSP00000513850.1:n.-33G>C
ENST00000376701.5:c.-33G>C MANE Select ENSP00000365891.4:n.-33G>C
ENST00000376701.4:c.-33G>C ENSP00000365891.4:n.-33G>C
ENST00000450772.5:c.-33G>C ENSP00000410537.1:n.-33G>C
ENST00000465982.5:n.3G>C
NM_000377.2:c.-33G>C , LRG_125t1:c.-33G>C NP_000368.1:n.-33G>C
XM_011543977.1:c.-33G>C XP_011542279.1:n.-33G>C
XM_011543977.2:c.-33G>C XP_011542279.1:n.-33G>C
XM_017029786.1:c.-33G>C XP_016885275.1:n.-33G>C
NM_000377.3:c.-33G>C MANE Select NP_000368.1:n.-33G>C
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