Canonical Allele Identifier: CA2798720234
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32315527_32315528insTATTTGCAATGTATCC , CM000675.2:g.32315527_32315528insTATTTGCAATGTATCC GRCh38
NC_000013.10:g.32889664_32889665insTATTTGCAATGTATCC , CM000675.1:g.32889664_32889665insTATTTGCAATGTATCC GRCh37
NC_000013.9:g.31787664_31787665insTATTTGCAATGTATCC NCBI36
NG_012772.3:g.5048_5049insTATTTGCAATGTATCC , LRG_293:g.5048_5049insTATTTGCAATGTATCC
NG_017006.1:g.1428_1429insGATACATTGCAAATAG
NG_017006.2:g.4837_4838insGATACATTGCAAATAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.-180_-179insTATTTGCAATGTATCC ENSP00000434898.2:n.-180_-179insTATTTGCAATGTATCC
ENST00000528762.2:c.-180_-179insTATTTGCAATGTATCC ENSP00000433168.2:n.-180_-179insTATTTGCAATGTATCC
ENST00000530893.7:c.-545_-544insTATTTGCAATGTATCC ENSP00000499438.2:n.-545_-544insTATTTGCAATGTATCC
ENST00000665585.2:c.-180_-179insTATTTGCAATGTATCC ENSP00000499570.2:n.-180_-179insTATTTGCAATGTATCC
ENST00000666593.2:c.-180_-179insTATTTGCAATGTATCC ENSP00000499256.2:n.-180_-179insTATTTGCAATGTATCC
ENST00000700202.2:c.-180_-179insTATTTGCAATGTATCC ENSP00000514856.2:n.-180_-179insTATTTGCAATGTATCC
ENST00000380152.8:c.-180_-179insTATTTGCAATGTATCC MANE Select ENSP00000369497.3:n.-180_-179insTATTTGCAATGTATCC
ENST00000544455.6:c.-40+382_-40+383insTATTTGCAATGTATCC ENSP00000439902.1:n.-40+382_-40+383insTATTTGCAATGTATCC
ENST00000380152.7:c.-180_-179insTATTTGCAATGTATCC ENSP00000369497.3:n.-180_-179insTATTTGCAATGTATCC
ENST00000530893.6:n.23_24insTATTTGCAATGTATCC
ENST00000544455.5:c.-180_-179insTATTTGCAATGTATCC ENSP00000439902.1:n.-180_-179insTATTTGCAATGTATCC
NM_000059.3:c.-180_-179insTATTTGCAATGTATCC , LRG_293t1:c.-180_-179insTATTTGCAATGTATCC NP_000050.2:n.-180_-179insTATTTGCAATGTATCC
XM_011535203.1:c.-40+382_-40+383insTATTTGCAATGTATCC XP_011533505.1:n.-40+382_-40+383insTATTTGCAATGTATCC
XM_011535204.1:c.-180_-179insTATTTGCAATGTATCC XP_011533506.1:n.-180_-179insTATTTGCAATGTATCC
XM_011535205.1:c.-180_-179insTATTTGCAATGTATCC XP_011533507.1:n.-180_-179insTATTTGCAATGTATCC
NM_000059.4:c.-180_-179insTATTTGCAATGTATCC MANE Select NP_000050.3:n.-180_-179insTATTTGCAATGTATCC