Canonical Allele Identifier: CA331093733

Gene: BRWD3

Linked Data

• dbSNP Id: rs746352783
• gnomAD v3: X-80745808-GACAAA-G
• gnomAD v4: X-80745808-GACAAA-G
• MyVariant Identifiers: chrX:g.80001308_80001312del (hg19) ; chrX:g.80745809_80745813del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745812_80745816del , CM000685.2:g.80745812_80745816del	GRCh38
NC_000023.10:g.80001311_80001315del , CM000685.1:g.80001311_80001315del	GRCh37
NC_000023.9:g.79887967_79887971del	NCBI36
NG_021349.1:g.68922_68926del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373275.5:c.431-84_431-80del MANE Select	ENSP00000362372.4:n.431-84_431-80del
ENST00000373275.4:c.431-84_431-80del	ENSP00000362372.4:n.431-84_431-80del
ENST00000478415.1:n.643-84_643-80del
NM_153252.4:c.431-84_431-80del	NP_694984.4:n.431-84_431-80del
XM_005262113.2:c.431-84_431-80del	XP_005262170.1:n.431-84_431-80del
XM_011530903.1:c.-83-84_-83-80del	XP_011529205.1:n.-83-84_-83-80del
XM_011530904.1:c.-906-84_-906-80del	XP_011529206.1:n.-906-84_-906-80del
XR_430519.2:n.694-84_694-80del
XM_005262113.3:c.431-84_431-80del	XP_005262170.1:n.431-84_431-80del
XM_017029384.1:c.-906-84_-906-80del	XP_016884873.1:n.-906-84_-906-80del
XM_017029385.2:c.431-84_431-80del	XP_016884874.1:n.431-84_431-80del
XR_430519.3:n.696-84_696-80del
NM_153252.5:c.431-84_431-80del MANE Select	NP_694984.5:n.431-84_431-80del