Canonical Allele Identifier: CA2499222107

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 1172110
• ClinVar RCV Id: RCV001525731
• dbSNP Id: rs2137487466

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32336888_32336889delinsGA , CM000675.2:g.32336888_32336889delinsGA	GRCh38
NC_000013.10:g.32911025_32911026delinsGA , CM000675.1:g.32911025_32911026delinsGA	GRCh37
NC_000013.9:g.31809025_31809026delinsGA	NCBI36
NG_012772.3:g.26409_26410delinsGA , LRG_293:g.26409_26410delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.2533_2534delinsGA	ENSP00000434898.2:p.Pro845Asp
ENST00000528762.2:c.2533_2534delinsGA	ENSP00000433168.2:p.Pro845Asp
ENST00000530893.7:c.2164_2165delinsGA	ENSP00000499438.2:p.Pro722Asp
ENST00000665585.2:c.2533_2534delinsGA	ENSP00000499570.2:p.Pro845Asp
ENST00000666593.2:c.2533_2534delinsGA	ENSP00000499256.2:p.Pro845Asp
ENST00000700202.2:c.2533_2534delinsGA	ENSP00000514856.2:p.Pro845Asp
ENST00000380152.8:c.2533_2534delinsGA MANE Select	ENSP00000369497.3:p.Pro845Asp
ENST00000544455.6:c.2533_2534delinsGA	ENSP00000439902.1:p.Pro845Asp
ENST00000614259.2:c.2533_2534delinsGA	ENSP00000506251.1:p.Pro845Asp
ENST00000680887.1:c.2533_2534delinsGA	ENSP00000505508.1:p.Pro845Asp
ENST00000380152.7:c.2533_2534delinsGA	ENSP00000369497.3:p.Pro845Asp
ENST00000544455.5:c.2533_2534delinsGA	ENSP00000439902.1:p.Pro845Asp
ENST00000614259.1:n.2533_2534delinsGA
NM_000059.3:c.2533_2534delinsGA , LRG_293t1:c.2533_2534delinsGA	NP_000050.2:p.Pro845Asp
XM_011535203.1:c.2533_2534delinsGA	XP_011533505.1:p.Pro845Asp
XM_011535204.1:c.2533_2534delinsGA	XP_011533506.1:p.Pro845Asp
XM_011535205.1:c.2533_2534delinsGA	XP_011533507.1:p.Pro845Asp
NM_000059.4:c.2533_2534delinsGA MANE Select	NP_000050.3:p.Pro845Asp