Canonical Allele Identifier: CA413607374

Gene: BRWD3

Linked Data

• MyVariant Identifiers: chrX:g.80001096A>T (hg19) ; chrX:g.80745597A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80745597A>T , CM000685.2:g.80745597A>T	GRCh38
NC_000023.10:g.80001096A>T , CM000685.1:g.80001096A>T	GRCh37
NC_000023.9:g.79887752A>T	NCBI36
NG_021349.1:g.69138T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000373275.5:c.563T>A MANE Select	ENSP00000362372.4:p.Phe188Tyr
ENST00000373275.4:c.563T>A	ENSP00000362372.4:p.Phe188Tyr
ENST00000478415.1:n.775T>A
NM_153252.4:c.563T>A	NP_694984.4:p.Phe188Tyr
XM_005262113.2:c.563T>A	XP_005262170.1:p.Phe188Tyr
XM_011530903.1:c.50T>A	XP_011529205.1:p.Phe17Tyr
XM_011530904.1:c.-774T>A	XP_011529206.1:n.-774T>A
XR_430519.2:n.826T>A
XM_005262113.3:c.563T>A	XP_005262170.1:p.Phe188Tyr
XM_017029384.1:c.-774T>A	XP_016884873.1:n.-774T>A
XM_017029385.2:c.563T>A	XP_016884874.1:p.Phe188Tyr
XR_430519.3:n.828T>A
NM_153252.5:c.563T>A MANE Select	NP_694984.5:p.Phe188Tyr