Canonical Allele Identifier: CA2440263099

Gene: BRWD3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745888A= , CM000685.2:g.80745888A=	GRCh38
NC_000023.10:g.80001387A= , CM000685.1:g.80001387A=	GRCh37
NC_000023.9:g.79888043A=	NCBI36
NG_021349.1:g.68847T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373275.5:c.431-159T= MANE Select	ENSP00000362372.4:n.431-159T=
ENST00000373275.4:c.431-159T=	ENSP00000362372.4:n.431-159T=
ENST00000478415.1:n.643-159T=
NM_153252.4:c.431-159T=	NP_694984.4:n.431-159T=
XM_005262113.2:c.431-159T=	XP_005262170.1:n.431-159T=
XM_011530903.1:c.-83-159T=	XP_011529205.1:n.-83-159T=
XM_011530904.1:c.-906-159T=	XP_011529206.1:n.-906-159T=
XR_430519.2:n.694-159T=
XM_005262113.3:c.431-159T=	XP_005262170.1:n.431-159T=
XM_017029384.1:c.-906-159T=	XP_016884873.1:n.-906-159T=
XM_017029385.2:c.431-159T=	XP_016884874.1:n.431-159T=
XR_430519.3:n.696-159T=
NM_153252.5:c.431-159T= MANE Select	NP_694984.5:n.431-159T=