Canonical Allele Identifier: CA2440263042

Gene: BRWD3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745707T= , CM000685.2:g.80745707T=	GRCh38
NC_000023.10:g.80001206T= , CM000685.1:g.80001206T=	GRCh37
NC_000023.9:g.79887862T=	NCBI36
NG_021349.1:g.69028A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373275.5:c.453A= MANE Select	ENSP00000362372.4:p.Gln151=
ENST00000373275.4:c.453A=	ENSP00000362372.4:p.Gln151=
ENST00000478415.1:n.665A=
NM_153252.4:c.453A=	NP_694984.4:p.Gln151=
XM_005262113.2:c.453A=	XP_005262170.1:p.Gln151=
XM_011530903.1:c.-61A=	XP_011529205.1:n.-61A=
XM_011530904.1:c.-884A=	XP_011529206.1:n.-884A=
XR_430519.2:n.716A=
XM_005262113.3:c.453A=	XP_005262170.1:p.Gln151=
XM_017029384.1:c.-884A=	XP_016884873.1:n.-884A=
XM_017029385.2:c.453A=	XP_016884874.1:p.Gln151=
XR_430519.3:n.718A=
NM_153252.5:c.453A= MANE Select	NP_694984.5:p.Gln151=