Canonical Allele Identifier: CA878678263

Gene: BRWD3

Linked Data

• dbSNP Id: rs1411211388
• MyVariant Identifiers: chrX:g.80001286_80001287del (hg19) ; chrX:g.80745787_80745788del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745787_80745788del , CM000685.2:g.80745787_80745788del	GRCh38
NC_000023.10:g.80001286_80001287del , CM000685.1:g.80001286_80001287del	GRCh37
NC_000023.9:g.79887942_79887943del	NCBI36
NG_021349.1:g.68947_68948del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373275.5:c.431-59_431-58del MANE Select	ENSP00000362372.4:n.431-59_431-58del
ENST00000373275.4:c.431-59_431-58del	ENSP00000362372.4:n.431-59_431-58del
ENST00000478415.1:n.643-59_643-58del
NM_153252.4:c.431-59_431-58del	NP_694984.4:n.431-59_431-58del
XM_005262113.2:c.431-59_431-58del	XP_005262170.1:n.431-59_431-58del
XM_011530903.1:c.-83-59_-83-58del	XP_011529205.1:n.-83-59_-83-58del
XM_011530904.1:c.-906-59_-906-58del	XP_011529206.1:n.-906-59_-906-58del
XR_430519.2:n.694-59_694-58del
XM_005262113.3:c.431-59_431-58del	XP_005262170.1:n.431-59_431-58del
XM_017029384.1:c.-906-59_-906-58del	XP_016884873.1:n.-906-59_-906-58del
XM_017029385.2:c.431-59_431-58del	XP_016884874.1:n.431-59_431-58del
XR_430519.3:n.696-59_696-58del
NM_153252.5:c.431-59_431-58del MANE Select	NP_694984.5:n.431-59_431-58del