Canonical Allele Identifier: CA517056278

Gene: BRWD3

Linked Data

• MyVariant Identifiers: chrX:g.80001092G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745593G>A , CM000685.2:g.80745593G>A	GRCh38
NC_000023.10:g.80001092G>A , CM000685.1:g.80001092G>A	GRCh37
NC_000023.9:g.79887748G>A	NCBI36
NG_021349.1:g.69142C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000373275.5:c.567C>T MANE Select	ENSP00000362372.4:p.Asp189=
ENST00000373275.4:c.567C>T	ENSP00000362372.4:p.Asp189=
ENST00000478415.1:n.779C>T
NM_153252.4:c.567C>T	NP_694984.4:p.Asp189=
XM_005262113.2:c.567C>T	XP_005262170.1:p.Asp189=
XM_011530903.1:c.54C>T	XP_011529205.1:p.Asp18=
XM_011530904.1:c.-770C>T	XP_011529206.1:n.-770C>T
XR_430519.2:n.830C>T
XM_005262113.3:c.567C>T	XP_005262170.1:p.Asp189=
XM_017029384.1:c.-770C>T	XP_016884873.1:n.-770C>T
XM_017029385.2:c.567C>T	XP_016884874.1:p.Asp189=
XR_430519.3:n.832C>T
NM_153252.5:c.567C>T MANE Select	NP_694984.5:p.Asp189=