Canonical Allele Identifier: CA517056393

Gene: BRWD3

Linked Data

• MyVariant Identifiers: chrX:g.80001221G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745722G>T , CM000685.2:g.80745722G>T	GRCh38
NC_000023.10:g.80001221G>T , CM000685.1:g.80001221G>T	GRCh37
NC_000023.9:g.79887877G>T	NCBI36
NG_021349.1:g.69013C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373275.5:c.438C>A MANE Select	ENSP00000362372.4:p.Ile146=
ENST00000373275.4:c.438C>A	ENSP00000362372.4:p.Ile146=
ENST00000478415.1:n.650C>A
NM_153252.4:c.438C>A	NP_694984.4:p.Ile146=
XM_005262113.2:c.438C>A	XP_005262170.1:p.Ile146=
XM_011530903.1:c.-76C>A	XP_011529205.1:n.-76C>A
XM_011530904.1:c.-899C>A	XP_011529206.1:n.-899C>A
XR_430519.2:n.701C>A
XM_005262113.3:c.438C>A	XP_005262170.1:p.Ile146=
XM_017029384.1:c.-899C>A	XP_016884873.1:n.-899C>A
XM_017029385.2:c.438C>A	XP_016884874.1:p.Ile146=
XR_430519.3:n.703C>A
NM_153252.5:c.438C>A MANE Select	NP_694984.5:p.Ile146=