Canonical Allele Identifier: CA607358406

Gene: BRAP

Linked Data

• dbSNP Id: rs80154506
• gnomAD v2: 12-112119174-C-CA
• gnomAD v3: 12-111681370-C-CA
• gnomAD v4: 12-111681370-C-CA
• MyVariant Identifiers: chr12:g.112119176_112119177insA (hg19) ; chr12:g.112119174_112119175insA (hg19) ; chr12:g.111681372_111681373insA (hg38) ; chr12:g.111681370_111681371insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111681383dup , CM000674.2:g.111681383dup	GRCh38
NC_000012.11:g.112119187dup , CM000674.1:g.112119187dup	GRCh37
NC_000012.10:g.110603570dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000419234.9:c.443+266dup MANE Select	ENSP00000403524.3:n.443+266dup
ENST00000327551.6:c.353+266dup	ENSP00000330813.5:n.353+266dup
ENST00000419234.8:c.443+266dup	ENSP00000403524.3:n.443+266dup
NM_006768.4:c.443+266dup	NP_006759.3:n.443+266dup
XM_005253944.3:c.566+266dup	XP_005254001.1:n.566+266dup
XM_011538788.1:c.-5+1775dup	XP_011537090.1:n.-5+1775dup
XM_011538789.1:c.-270+266dup	XP_011537091.1:n.-270+266dup
XM_005253944.4:c.566+266dup	XP_005254001.1:n.566+266dup
XM_011538789.3:c.-270+266dup	XP_011537091.1:n.-270+266dup
XM_017019992.1:c.281+266dup	XP_016875481.1:n.281+266dup
XM_017019993.1:c.-5+1775dup	XP_016875482.1:n.-5+1775dup
XM_017019994.1:c.-4-2031dup	XP_016875483.1:n.-4-2031dup
NM_006768.5:c.443+266dup MANE Select	NP_006759.3:n.443+266dup