Canonical Allele Identifier: CA2798730068

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32370691_32370692insGGGCAAGAGACCAAAACCCCCAAA , CM000675.2:g.32370691_32370692insGGGCAAGAGACCAAAACCCCCAAA	GRCh38
NC_000013.10:g.32944828_32944829insGGGCAAGAGACCAAAACCCCCAAA , CM000675.1:g.32944828_32944829insGGGCAAGAGACCAAAACCCCCAAA	GRCh37
NC_000013.9:g.31842828_31842829insGGGCAAGAGACCAAAACCCCCAAA	NCBI36
NG_012772.3:g.60212_60213insGGGCAAGAGACCAAAACCCCCAAA , LRG_293:g.60212_60213insGGGCAAGAGACCAAAACCCCCAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8487+134_8487+135insGGGCAAGAGACCAAAACCCCCAAA	ENSP00000434898.2:n.8487+134_8487+135insGGGCAAGAGACCAAAACCCCC...
ENST00000528762.2:c.8487+134_8487+135insGGGCAAGAGACCAAAACCCCCAAA	ENSP00000433168.2:n.8487+134_8487+135insGGGCAAGAGACCAAAACCCCC...
ENST00000530893.7:c.8118+134_8118+135insGGGCAAGAGACCAAAACCCCCAAA	ENSP00000499438.2:n.8118+134_8118+135insGGGCAAGAGACCAAAACCCCC...
ENST00000665585.2:c.8487+134_8487+135insGGGCAAGAGACCAAAACCCCCAAA	ENSP00000499570.2:n.8487+134_8487+135insGGGCAAGAGACCAAAACCCCC...
ENST00000666593.2:c.8487+134_8487+135insGGGCAAGAGACCAAAACCCCCAAA	ENSP00000499256.2:n.8487+134_8487+135insGGGCAAGAGACCAAAACCCCC...
ENST00000700202.2:c.8487+134_8487+135insGGGCAAGAGACCAAAACCCCCAAA	ENSP00000514856.2:n.8487+134_8487+135insGGGCAAGAGACCAAAACCCCC...
ENST00000700202.1:c.954+134_954+135insGGGCAAGAGACCAAAACCCCCAAA	ENSP00000514856.1:n.954+134_954+135insGGGCAAGAGACCAAAACCCCCAA...
ENST00000380152.8:c.8487+134_8487+135insGGGCAAGAGACCAAAACCCCCAAA MANE Select	ENSP00000369497.3:n.8487+134_8487+135insGGGCAAGAGACCAAAACCCCC...
ENST00000544455.6:c.8487+134_8487+135insGGGCAAGAGACCAAAACCCCCAAA	ENSP00000439902.1:n.8487+134_8487+135insGGGCAAGAGACCAAAACCCCC...
ENST00000614259.2:c.8495+134_8495+135insGGGCAAGAGACCAAAACCCCCAAA	ENSP00000506251.1:n.8495+134_8495+135insGGGCAAGAGACCAAAACCCCC...
ENST00000665585.1:c.1052+134_1052+135insGGGCAAGAGACCAAAACCCCCAAA
ENST00000680887.1:c.8487+134_8487+135insGGGCAAGAGACCAAAACCCCCAAA	ENSP00000505508.1:n.8487+134_8487+135insGGGCAAGAGACCAAAACCCCC...
ENST00000380152.7:c.8487+134_8487+135insGGGCAAGAGACCAAAACCCCCAAA	ENSP00000369497.3:n.8487+134_8487+135insGGGCAAGAGACCAAAACCCCC...
ENST00000544455.5:c.8487+134_8487+135insGGGCAAGAGACCAAAACCCCCAAA	ENSP00000439902.1:n.8487+134_8487+135insGGGCAAGAGACCAAAACCCCC...
NM_000059.3:c.8487+134_8487+135insGGGCAAGAGACCAAAACCCCCAAA , LRG_293t1:c.8487+134_8487+135insGGGCAAGAGACCAAAACCCCCAAA	NP_000050.2:n.8487+134_8487+135insGGGCAAGAGACCAAAACCCCCAAA
XM_011535203.1:c.8487+134_8487+135insGGGCAAGAGACCAAAACCCCCAAA	XP_011533505.1:n.8487+134_8487+135insGGGCAAGAGACCAAAACCCCCAAA...
XM_011535204.1:c.8391+134_8391+135insGGGCAAGAGACCAAAACCCCCAAA	XP_011533506.1:n.8391+134_8391+135insGGGCAAGAGACCAAAACCCCCAAA...
XM_011535205.1:c.8487+134_8487+135insGGGCAAGAGACCAAAACCCCCAAA	XP_011533507.1:n.8487+134_8487+135insGGGCAAGAGACCAAAACCCCCAAA...
NM_000059.4:c.8487+134_8487+135insGGGCAAGAGACCAAAACCCCCAAA MANE Select	NP_000050.3:n.8487+134_8487+135insGGGCAAGAGACCAAAACCCCCAAA