Canonical Allele Identifier: CA2550864348
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32380440_32380443del , CM000675.2:g.32380440_32380443del GRCh38
NC_000013.10:g.32954577_32954580del , CM000675.1:g.32954577_32954580del GRCh37
NC_000013.9:g.31852577_31852580del NCBI36
NG_012772.3:g.69961_69964del , LRG_293:g.69961_69964del

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.9256+295_9256+298del ENSP00000434898.2:n.9256+295_9256+298del
ENST00000528762.2:c.*623+295_*623+298del ENSP00000433168.2:n.*623+295_*623+298del
ENST00000530893.7:c.8887+295_8887+298del ENSP00000499438.2:n.8887+295_8887+298del
ENST00000665585.2:c.*818+295_*818+298del ENSP00000499570.2:n.*818+295_*818+298del
ENST00000666593.2:c.9256+295_9256+298del ENSP00000499256.2:n.9256+295_9256+298del
ENST00000700202.2:c.9205+295_9205+298del ENSP00000514856.2:n.9205+295_9205+298del
ENST00000700202.1:c.1672+295_1672+298del ENSP00000514856.1:n.1672+295_1672+298del
ENST00000700203.1:n.1383+295_1383+298del
ENST00000380152.8:c.9256+295_9256+298del MANE Select ENSP00000369497.3:n.9256+295_9256+298del
ENST00000544455.6:c.9256+295_9256+298del ENSP00000439902.1:n.9256+295_9256+298del
ENST00000614259.2:c.9264+295_9264+298del ENSP00000506251.1:n.9264+295_9264+298del
ENST00000665585.1:c.2134+295_2134+298del
ENST00000666593.1:c.139+295_139+298del ENSP00000499256.1:n.139+295_139+298del
ENST00000680887.1:c.9256+295_9256+298del ENSP00000505508.1:n.9256+295_9256+298del
ENST00000380152.7:c.9256+295_9256+298del ENSP00000369497.3:n.9256+295_9256+298del
ENST00000470094.1:c.213+295_213+298del
ENST00000544455.5:c.9256+295_9256+298del ENSP00000439902.1:n.9256+295_9256+298del
NM_000059.3:c.9256+295_9256+298del , LRG_293t1:c.9256+295_9256+298del NP_000050.2:n.9256+295_9256+298del
XM_011535203.1:c.9256+295_9256+298del XP_011533505.1:n.9256+295_9256+298del
XM_011535204.1:c.9160+295_9160+298del XP_011533506.1:n.9160+295_9160+298del
NM_000059.4:c.9256+295_9256+298del MANE Select NP_000050.3:n.9256+295_9256+298del