Canonical Allele Identifier: CA2622600252

Gene: BRCA2

Linked Data

• gnomAD v4: 13-32331151-C-CAG

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32331151_32331152insAG , CM000675.2:g.32331151_32331152insAG	GRCh38
NC_000013.10:g.32905288_32905289insAG , CM000675.1:g.32905288_32905289insAG	GRCh37
NC_000013.9:g.31803288_31803289insAG	NCBI36
NG_012772.3:g.20672_20673insAG , LRG_293:g.20672_20673insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.793+121_793+122insAG	ENSP00000434898.2:n.793+121_793+122insAG
ENST00000528762.2:c.793+121_793+122insAG	ENSP00000433168.2:n.793+121_793+122insAG
ENST00000530893.7:c.424+121_424+122insAG	ENSP00000499438.2:n.424+121_424+122insAG
ENST00000665585.2:c.793+121_793+122insAG	ENSP00000499570.2:n.793+121_793+122insAG
ENST00000666593.2:c.793+121_793+122insAG	ENSP00000499256.2:n.793+121_793+122insAG
ENST00000700202.2:c.793+121_793+122insAG	ENSP00000514856.2:n.793+121_793+122insAG
ENST00000700201.1:c.*572+121_*572+122insAG	ENSP00000514855.1:n.*572+121_*572+122insAG
ENST00000380152.8:c.793+121_793+122insAG MANE Select	ENSP00000369497.3:n.793+121_793+122insAG
ENST00000544455.6:c.793+121_793+122insAG	ENSP00000439902.1:n.793+121_793+122insAG
ENST00000614259.2:c.793+121_793+122insAG	ENSP00000506251.1:n.793+121_793+122insAG
ENST00000680887.1:c.793+121_793+122insAG	ENSP00000505508.1:n.793+121_793+122insAG
ENST00000380152.7:c.793+121_793+122insAG	ENSP00000369497.3:n.793+121_793+122insAG
ENST00000530893.6:n.991+121_991+122insAG
ENST00000544455.5:c.793+121_793+122insAG	ENSP00000439902.1:n.793+121_793+122insAG
ENST00000614259.1:n.793+121_793+122insAG
NM_000059.3:c.793+121_793+122insAG , LRG_293t1:c.793+121_793+122insAG	NP_000050.2:n.793+121_793+122insAG
XM_011535203.1:c.793+121_793+122insAG	XP_011533505.1:n.793+121_793+122insAG
XM_011535204.1:c.793+121_793+122insAG	XP_011533506.1:n.793+121_793+122insAG
XM_011535205.1:c.793+121_793+122insAG	XP_011533507.1:n.793+121_793+122insAG
NM_000059.4:c.793+121_793+122insAG MANE Select	NP_000050.3:n.793+121_793+122insAG