Canonical Allele Identifier: CA2440263068

Gene: BRWD3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745786_80745788delinsTAA , CM000685.2:g.80745786_80745788delinsTAA	GRCh38
NC_000023.10:g.80001285_80001287delinsTAA , CM000685.1:g.80001285_80001287delinsTAA	GRCh37
NC_000023.9:g.79887941_79887943delinsTAA	NCBI36
NG_021349.1:g.68947_68949delinsTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373275.5:c.431-59_431-57delinsTTA MANE Select	ENSP00000362372.4:n.431-59_431-57delinsTTA
ENST00000373275.4:c.431-59_431-57delinsTTA	ENSP00000362372.4:n.431-59_431-57delinsTTA
ENST00000478415.1:n.643-59_643-57delinsTTA
NM_153252.4:c.431-59_431-57delinsTTA	NP_694984.4:n.431-59_431-57delinsTTA
XM_005262113.2:c.431-59_431-57delinsTTA	XP_005262170.1:n.431-59_431-57delinsTTA
XM_011530903.1:c.-83-59_-83-57delinsTTA	XP_011529205.1:n.-83-59_-83-57delinsTTA
XM_011530904.1:c.-906-59_-906-57delinsTTA	XP_011529206.1:n.-906-59_-906-57delinsTTA
XR_430519.2:n.694-59_694-57delinsTTA
XM_005262113.3:c.431-59_431-57delinsTTA	XP_005262170.1:n.431-59_431-57delinsTTA
XM_017029384.1:c.-906-59_-906-57delinsTTA	XP_016884873.1:n.-906-59_-906-57delinsTTA
XM_017029385.2:c.431-59_431-57delinsTTA	XP_016884874.1:n.431-59_431-57delinsTTA
XR_430519.3:n.696-59_696-57delinsTTA
NM_153252.5:c.431-59_431-57delinsTTA MANE Select	NP_694984.5:n.431-59_431-57delinsTTA