Canonical Allele Identifier: CA2063407734

Gene: BRAP

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111681379A= , CM000674.2:g.111681379A=	GRCh38
NC_000012.11:g.112119183A= , CM000674.1:g.112119183A=	GRCh37
NC_000012.10:g.110603566A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000419234.9:c.443+258T= MANE Select	ENSP00000403524.3:n.443+258T=
ENST00000327551.6:c.353+258T=	ENSP00000330813.5:n.353+258T=
ENST00000419234.8:c.443+258T=	ENSP00000403524.3:n.443+258T=
NM_006768.4:c.443+258T=	NP_006759.3:n.443+258T=
XM_005253944.3:c.566+258T=	XP_005254001.1:n.566+258T=
XM_011538788.1:c.-5+1767T=	XP_011537090.1:n.-5+1767T=
XM_011538789.1:c.-270+258T=	XP_011537091.1:n.-270+258T=
XM_005253944.4:c.566+258T=	XP_005254001.1:n.566+258T=
XM_011538789.3:c.-270+258T=	XP_011537091.1:n.-270+258T=
XM_017019992.1:c.281+258T=	XP_016875481.1:n.281+258T=
XM_017019993.1:c.-5+1767T=	XP_016875482.1:n.-5+1767T=
XM_017019994.1:c.-4-2039T=	XP_016875483.1:n.-4-2039T=
NM_006768.5:c.443+258T= MANE Select	NP_006759.3:n.443+258T=