Canonical Allele Identifier: CA2727218607

Gene: BRAP

Linked Data

• dbSNP Id: rs2135931012

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111681393T>G , CM000674.2:g.111681393T>G	GRCh38
NC_000012.11:g.112119197T>G , CM000674.1:g.112119197T>G	GRCh37
NC_000012.10:g.110603580T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000419234.9:c.443+244A>C MANE Select	ENSP00000403524.3:n.443+244A>C
ENST00000327551.6:c.353+244A>C	ENSP00000330813.5:n.353+244A>C
ENST00000419234.8:c.443+244A>C	ENSP00000403524.3:n.443+244A>C
NM_006768.4:c.443+244A>C	NP_006759.3:n.443+244A>C
XM_005253944.3:c.566+244A>C	XP_005254001.1:n.566+244A>C
XM_011538788.1:c.-5+1753A>C	XP_011537090.1:n.-5+1753A>C
XM_011538789.1:c.-270+244A>C	XP_011537091.1:n.-270+244A>C
XM_005253944.4:c.566+244A>C	XP_005254001.1:n.566+244A>C
XM_011538789.3:c.-270+244A>C	XP_011537091.1:n.-270+244A>C
XM_017019992.1:c.281+244A>C	XP_016875481.1:n.281+244A>C
XM_017019993.1:c.-5+1753A>C	XP_016875482.1:n.-5+1753A>C
XM_017019994.1:c.-4-2053A>C	XP_016875483.1:n.-4-2053A>C
NM_006768.5:c.443+244A>C MANE Select	NP_006759.3:n.443+244A>C