Canonical Allele Identifier: CA2622600111

Gene: BRCA2

Linked Data

• gnomAD v4: 13-32339554-C-CTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32339554_32339555insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG , CM000675.2:g.32339554_32339555insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG	GRCh38
NC_000013.10:g.32913691_32913692insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG , CM000675.1:g.32913691_32913692insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG	GRCh37
NC_000013.9:g.31811691_31811692insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG	NCBI36
NG_012772.3:g.29075_29076insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG , LRG_293:g.29075_29076insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.5199_5200insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG	ENSP00000434898.2:p.Glu1734CysfsTer8
ENST00000528762.2:c.5199_5200insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG	ENSP00000433168.2:p.Glu1734CysfsTer8
ENST00000530893.7:c.4830_4831insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG	ENSP00000499438.2:p.Glu1611CysfsTer8
ENST00000665585.2:c.5199_5200insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG	ENSP00000499570.2:p.Glu1734CysfsTer8
ENST00000666593.2:c.5199_5200insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG	ENSP00000499256.2:p.Glu1734CysfsTer8
ENST00000700202.2:c.5199_5200insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG	ENSP00000514856.2:p.Glu1734CysfsTer8
ENST00000380152.8:c.5199_5200insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG MANE Select	ENSP00000369497.3:p.Glu1734CysfsTer8
ENST00000544455.6:c.5199_5200insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG	ENSP00000439902.1:p.Glu1734CysfsTer8
ENST00000614259.2:c.5199_5200insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG	ENSP00000506251.1:p.Glu1734CysfsTer8
ENST00000680887.1:c.5199_5200insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG	ENSP00000505508.1:p.Glu1734CysfsTer8
ENST00000380152.7:c.5199_5200insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG	ENSP00000369497.3:p.Glu1734CysfsTer8
ENST00000544455.5:c.5199_5200insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG	ENSP00000439902.1:p.Glu1734CysfsTer8
ENST00000614259.1:n.5199_5200insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG
NM_000059.3:c.5199_5200insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG , LRG_293t1:c.5199_5200insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG	NP_000050.2:p.Glu1734CysfsTer8
XM_011535203.1:c.5199_5200insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG	XP_011533505.1:p.Glu1734CysfsTer8
XM_011535204.1:c.5199_5200insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG	XP_011533506.1:p.Glu1734CysfsTer8
XM_011535205.1:c.5199_5200insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG	XP_011533507.1:p.Glu1734CysfsTer8
NM_000059.4:c.5199_5200insTGCAAATACTTGTGGGATTTTTAGCACAGCAAGTG MANE Select	NP_000050.3:p.Glu1734CysfsTer8