Canonical Allele Identifier: CA10462359
Gene: BRWD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 713800
ClinVar RCV Id: RCV000885994
dbSNP Id: rs774454877
ExAC: X:80001231 G / GA
gnomAD v2: X-80001231-G-GA
gnomAD v3: X-80745732-G-GA
gnomAD v4: X-80745732-G-GA
MyVariant Identifiers: chrX:g.80001231_80001232insA (hg19) chrX:g.80745732_80745733insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.80745739dup , CM000685.2:g.80745739dup GRCh38
NC_000023.10:g.80001238dup , CM000685.1:g.80001238dup GRCh37
NC_000023.9:g.79887894dup NCBI36
NG_021349.1:g.69002dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000373275.5:c.431-4dup MANE Select ENSP00000362372.4:n.431-4dup
ENST00000373275.4:c.431-4dup ENSP00000362372.4:n.431-4dup
ENST00000478415.1:n.643-4dup
NM_153252.4:c.431-4dup NP_694984.4:n.431-4dup
XM_005262113.2:c.431-4dup XP_005262170.1:n.431-4dup
XM_011530903.1:c.-83-4dup XP_011529205.1:n.-83-4dup
XM_011530904.1:c.-906-4dup XP_011529206.1:n.-906-4dup
XR_430519.2:n.694-4dup
XM_005262113.3:c.431-4dup XP_005262170.1:n.431-4dup
XM_017029384.1:c.-906-4dup XP_016884873.1:n.-906-4dup
XM_017029385.2:c.431-4dup XP_016884874.1:n.431-4dup
XR_430519.3:n.696-4dup
NM_153252.5:c.431-4dup MANE Select NP_694984.5:n.431-4dup
Search 100 bp 5'
Search 100 bp 3'