Canonical Allele Identifier: CA607358405

Gene: BRAP

Linked Data

• gnomAD v2: 12-112119173-T-A
• gnomAD v3: 12-111681369-T-A
• gnomAD v4: 12-111681369-T-A
• MyVariant Identifiers: chr12:g.112119173T>A (hg19) ; chr12:g.111681369T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111681369T>A , CM000674.2:g.111681369T>A	GRCh38
NC_000012.11:g.112119173T>A , CM000674.1:g.112119173T>A	GRCh37
NC_000012.10:g.110603556T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000419234.9:c.443+268A>T MANE Select	ENSP00000403524.3:n.443+268A>T
ENST00000327551.6:c.353+268A>T	ENSP00000330813.5:n.353+268A>T
ENST00000419234.8:c.443+268A>T	ENSP00000403524.3:n.443+268A>T
NM_006768.4:c.443+268A>T	NP_006759.3:n.443+268A>T
XM_005253944.3:c.566+268A>T	XP_005254001.1:n.566+268A>T
XM_011538788.1:c.-5+1777A>T	XP_011537090.1:n.-5+1777A>T
XM_011538789.1:c.-270+268A>T	XP_011537091.1:n.-270+268A>T
XM_005253944.4:c.566+268A>T	XP_005254001.1:n.566+268A>T
XM_011538789.3:c.-270+268A>T	XP_011537091.1:n.-270+268A>T
XM_017019992.1:c.281+268A>T	XP_016875481.1:n.281+268A>T
XM_017019993.1:c.-5+1777A>T	XP_016875482.1:n.-5+1777A>T
XM_017019994.1:c.-4-2029A>T	XP_016875483.1:n.-4-2029A>T
NM_006768.5:c.443+268A>T MANE Select	NP_006759.3:n.443+268A>T