Canonical Allele Identifier: CA10026671

Gene: BRWD1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.39202379A>G , CM000683.2:g.39202379A>G	GRCh38
NC_000021.8:g.40574305A>G , CM000683.1:g.40574305A>G	GRCh37
NC_000021.7:g.39496175A>G	NCBI36
NG_029919.1:g.116408T>C
NG_029919.2:g.116408T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342449.8:c.4531T>C MANE Select	ENSP00000344333.3:p.Ser1511Pro
ENST00000333229.6:c.4531T>C	ENSP00000330753.2:p.Ser1511Pro
ENST00000342449.7:c.4531T>C	ENSP00000344333.3:p.Ser1511Pro
ENST00000380800.7:c.4531T>C	ENSP00000370178.3:p.Ser1511Pro
ENST00000424441.1:c.1343T>C
ENST00000446924.5:c.2778T>C	ENSP00000391014.1:n.2778T>C
NM_018963.4:c.4531T>C	NP_061836.2:p.Ser1511Pro
NM_033656.3:c.4531T>C	NP_387505.1:p.Ser1511Pro
XM_011529611.1:c.4387T>C	XP_011527913.1:p.Ser1463Pro
XM_011529612.1:c.3691T>C	XP_011527914.1:p.Ser1231Pro
XM_011529613.1:c.1564T>C	XP_011527915.1:p.Ser522Pro
XM_011529612.2:c.3691T>C	XP_011527914.1:p.Ser1231Pro
XM_017028373.1:c.4270T>C	XP_016883862.1:p.Ser1424Pro
XM_017028374.1:c.1564T>C	XP_016883863.1:p.Ser522Pro
NM_018963.5:c.4531T>C	NP_061836.2:p.Ser1511Pro
NM_033656.4:c.4531T>C MANE Select	NP_387505.1:p.Ser1511Pro