Canonical Allele Identifier: CA10462367

Gene: BRWD3

Linked Data

• dbSNP Id: rs761879695
• ExAC: X:80001257 CTTAAAAG / C
• gnomAD v2: X-80001257-CTTAAAAG-C
• gnomAD v3: X-80745758-CTTAAAAG-C
• gnomAD v4: X-80745758-CTTAAAAG-C
• MyVariant Identifiers: chrX:g.80001258_80001264del (hg19) ; chrX:g.80745759_80745765del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745760_80745766del , CM000685.2:g.80745760_80745766del	GRCh38
NC_000023.10:g.80001259_80001265del , CM000685.1:g.80001259_80001265del	GRCh37
NC_000023.9:g.79887915_79887921del	NCBI36
NG_021349.1:g.68970_68976del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373275.5:c.431-36_431-30del MANE Select	ENSP00000362372.4:n.431-36_431-30del
ENST00000373275.4:c.431-36_431-30del	ENSP00000362372.4:n.431-36_431-30del
ENST00000478415.1:n.643-36_643-30del
NM_153252.4:c.431-36_431-30del	NP_694984.4:n.431-36_431-30del
XM_005262113.2:c.431-36_431-30del	XP_005262170.1:n.431-36_431-30del
XM_011530903.1:c.-83-36_-83-30del	XP_011529205.1:n.-83-36_-83-30del
XM_011530904.1:c.-906-36_-906-30del	XP_011529206.1:n.-906-36_-906-30del
XR_430519.2:n.694-36_694-30del
XM_005262113.3:c.431-36_431-30del	XP_005262170.1:n.431-36_431-30del
XM_017029384.1:c.-906-36_-906-30del	XP_016884873.1:n.-906-36_-906-30del
XM_017029385.2:c.431-36_431-30del	XP_016884874.1:n.431-36_431-30del
XR_430519.3:n.696-36_696-30del
NM_153252.5:c.431-36_431-30del MANE Select	NP_694984.5:n.431-36_431-30del