Canonical Allele Identifier: CA2063411861

Gene: BRAP

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111685480A>C , CM000674.2:g.111685480A>C	GRCh38
NC_000012.11:g.112123284A>C , CM000674.1:g.112123284A>C	GRCh37
NC_000012.10:g.110607667A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419234.9:c.82+231T>G MANE Select	ENSP00000403524.3:n.82+231T>G
ENST00000327551.6:c.-9+108T>G	ENSP00000330813.5:n.-9+108T>G
ENST00000419234.8:c.82+231T>G	ENSP00000403524.3:n.82+231T>G
NM_006768.4:c.82+231T>G	NP_006759.3:n.82+231T>G
XM_005253944.3:c.205+108T>G	XP_005254001.1:n.205+108T>G
XM_011538789.1:c.-631+231T>G	XP_011537091.1:n.-631+231T>G
XM_005253944.4:c.205+108T>G	XP_005254001.1:n.205+108T>G
XM_011538789.3:c.-631+231T>G	XP_011537091.1:n.-631+231T>G
XM_017019992.1:c.82+231T>G	XP_016875481.1:n.82+231T>G
XM_017019993.1:c.-167+231T>G	XP_016875482.1:n.-167+231T>G
XM_017019994.1:c.-5+231T>G	XP_016875483.1:n.-5+231T>G
NM_006768.5:c.82+231T>G MANE Select	NP_006759.3:n.82+231T>G