Canonical Allele Identifier: CA2822047243

Gene: BRWD3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745731_80745732del , CM000685.2:g.80745731_80745732del	GRCh38
NC_000023.10:g.80001230_80001231del , CM000685.1:g.80001230_80001231del	GRCh37
NC_000023.9:g.79887886_79887887del	NCBI36
NG_021349.1:g.69003_69004del

Transcript Alleles

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