Canonical Allele Identifier: CA331093714

Gene: BRWD3

Linked Data

• dbSNP Id: rs947398562
• gnomAD v3: X-80745748-TAACTTAA-T
• gnomAD v4: X-80745748-TAACTTAA-T
• MyVariant Identifiers: chrX:g.80001248_80001254del (hg19) ; chrX:g.80745749_80745755del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745758_80745764del , CM000685.2:g.80745758_80745764del	GRCh38
NC_000023.10:g.80001257_80001263del , CM000685.1:g.80001257_80001263del	GRCh37
NC_000023.9:g.79887913_79887919del	NCBI36
NG_021349.1:g.68980_68986del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373275.5:c.431-26_431-20del MANE Select	ENSP00000362372.4:n.431-26_431-20del
ENST00000373275.4:c.431-26_431-20del	ENSP00000362372.4:n.431-26_431-20del
ENST00000478415.1:n.643-26_643-20del
NM_153252.4:c.431-26_431-20del	NP_694984.4:n.431-26_431-20del
XM_005262113.2:c.431-26_431-20del	XP_005262170.1:n.431-26_431-20del
XM_011530903.1:c.-83-26_-83-20del	XP_011529205.1:n.-83-26_-83-20del
XM_011530904.1:c.-906-26_-906-20del	XP_011529206.1:n.-906-26_-906-20del
XR_430519.2:n.694-26_694-20del
XM_005262113.3:c.431-26_431-20del	XP_005262170.1:n.431-26_431-20del
XM_017029384.1:c.-906-26_-906-20del	XP_016884873.1:n.-906-26_-906-20del
XM_017029385.2:c.431-26_431-20del	XP_016884874.1:n.431-26_431-20del
XR_430519.3:n.696-26_696-20del
NM_153252.5:c.431-26_431-20del MANE Select	NP_694984.5:n.431-26_431-20del