Canonical Allele Identifier: CA2082747700
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32336258_32336264delinsTGTTTAG , CM000675.2:g.32336258_32336264delinsTGTTTAG GRCh38
NC_000013.10:g.32910395_32910401delinsTGTTTAG , CM000675.1:g.32910395_32910401delinsTGTTTAG GRCh37
NC_000013.9:g.31808395_31808401delinsTGTTTAG NCBI36
NG_012772.3:g.25779_25785delinsTGTTTAG , LRG_293:g.25779_25785delinsTGTTTAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.1910-7_1910-1delinsTGTTTAG ENSP00000434898.2:n.1910-7_1910-1delinsTGTTTAG
ENST00000528762.2:c.1910-7_1910-1delinsTGTTTAG ENSP00000433168.2:n.1910-7_1910-1delinsTGTTTAG
ENST00000530893.7:c.1541-7_1541-1delinsTGTTTAG ENSP00000499438.2:n.1541-7_1541-1delinsTGTTTAG
ENST00000665585.2:c.1910-7_1910-1delinsTGTTTAG ENSP00000499570.2:n.1910-7_1910-1delinsTGTTTAG
ENST00000666593.2:c.1910-7_1910-1delinsTGTTTAG ENSP00000499256.2:n.1910-7_1910-1delinsTGTTTAG
ENST00000700202.2:c.1910-7_1910-1delinsTGTTTAG ENSP00000514856.2:n.1910-7_1910-1delinsTGTTTAG
ENST00000380152.8:c.1910-7_1910-1delinsTGTTTAG MANE Select ENSP00000369497.3:n.1910-7_1910-1delinsTGTTTAG
ENST00000544455.6:c.1910-7_1910-1delinsTGTTTAG ENSP00000439902.1:n.1910-7_1910-1delinsTGTTTAG
ENST00000614259.2:c.1910-7_1910-1delinsTGTTTAG ENSP00000506251.1:n.1910-7_1910-1delinsTGTTTAG
ENST00000680887.1:c.1910-7_1910-1delinsTGTTTAG ENSP00000505508.1:n.1910-7_1910-1delinsTGTTTAG
ENST00000380152.7:c.1910-7_1910-1delinsTGTTTAG ENSP00000369497.3:n.1910-7_1910-1delinsTGTTTAG
ENST00000544455.5:c.1910-7_1910-1delinsTGTTTAG ENSP00000439902.1:n.1910-7_1910-1delinsTGTTTAG
ENST00000614259.1:n.1910-7_1910-1delinsTGTTTAG
NM_000059.3:c.1910-7_1910-1delinsTGTTTAG , LRG_293t1:c.1910-7_1910-1delinsTGTTTAG NP_000050.2:n.1910-7_1910-1delinsTGTTTAG
XM_011535203.1:c.1910-7_1910-1delinsTGTTTAG XP_011533505.1:n.1910-7_1910-1delinsTGTTTAG
XM_011535204.1:c.1910-7_1910-1delinsTGTTTAG XP_011533506.1:n.1910-7_1910-1delinsTGTTTAG
XM_011535205.1:c.1910-7_1910-1delinsTGTTTAG XP_011533507.1:n.1910-7_1910-1delinsTGTTTAG
NM_000059.4:c.1910-7_1910-1delinsTGTTTAG MANE Select NP_000050.3:n.1910-7_1910-1delinsTGTTTAG