Canonical Allele Identifier: CA386735438

Gene: BRAP

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111672685T>A , CM000674.2:g.111672685T>A	GRCh38
NC_000012.11:g.112110489T>A , CM000674.1:g.112110489T>A	GRCh37
NC_000012.10:g.110594872T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006768.5:c.723A>T MANE Select	NP_006759.3:p.Arg241Ser
ENST00000419234.9:c.723A>T MANE Select	ENSP00000403524.3:p.Arg241Ser
NM_006768.4:c.723A>T	NP_006759.3:p.Arg241Ser
ENST00000327551.6:c.633A>T	ENSP00000330813.5:p.Arg211Ser
ENST00000419234.8:c.723A>T	ENSP00000403524.3:p.Arg241Ser
ENST00000547043.1:n.627A>T
XM_005253944.3:c.846A>T	XP_005254001.1:p.Arg282Ser
XM_005253944.4:c.846A>T	XP_005254001.1:p.Arg282Ser
XM_011538788.1:c.276A>T	XP_011537090.1:p.Arg92Ser
XM_011538789.1:c.11A>T	XP_011537091.1:p.Glu4Val
XM_011538789.3:c.11A>T	XP_011537091.1:p.Glu4Val
XM_017019992.1:c.561A>T	XP_016875481.1:p.Arg187Ser
XM_017019993.1:c.276A>T	XP_016875482.1:p.Arg92Ser
XM_017019994.1:c.276A>T	XP_016875483.1:p.Arg92Ser
XM_017019995.1:c.276A>T	XP_016875484.1:p.Arg92Ser