Canonical Allele Identifier: CA607358408

Gene: BRAP

Linked Data

• dbSNP Id: rs1196428696
• gnomAD v2: 12-112119186-A-T
• gnomAD v3: 12-111681382-A-T
• gnomAD v4: 12-111681382-A-T
• MyVariant Identifiers: chr12:g.112119186A>T (hg19) ; chr12:g.111681382A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111681382A>T , CM000674.2:g.111681382A>T	GRCh38
NC_000012.11:g.112119186A>T , CM000674.1:g.112119186A>T	GRCh37
NC_000012.10:g.110603569A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000419234.9:c.443+255T>A MANE Select	ENSP00000403524.3:n.443+255T>A
ENST00000327551.6:c.353+255T>A	ENSP00000330813.5:n.353+255T>A
ENST00000419234.8:c.443+255T>A	ENSP00000403524.3:n.443+255T>A
NM_006768.4:c.443+255T>A	NP_006759.3:n.443+255T>A
XM_005253944.3:c.566+255T>A	XP_005254001.1:n.566+255T>A
XM_011538788.1:c.-5+1764T>A	XP_011537090.1:n.-5+1764T>A
XM_011538789.1:c.-270+255T>A	XP_011537091.1:n.-270+255T>A
XM_005253944.4:c.566+255T>A	XP_005254001.1:n.566+255T>A
XM_011538789.3:c.-270+255T>A	XP_011537091.1:n.-270+255T>A
XM_017019992.1:c.281+255T>A	XP_016875481.1:n.281+255T>A
XM_017019993.1:c.-5+1764T>A	XP_016875482.1:n.-5+1764T>A
XM_017019994.1:c.-4-2042T>A	XP_016875483.1:n.-4-2042T>A
NM_006768.5:c.443+255T>A MANE Select	NP_006759.3:n.443+255T>A