Canonical Allele Identifier: CA2082841553
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32380233_32380241delinsGTTGGCAAA , CM000675.2:g.32380233_32380241delinsGTTGGCAAA GRCh38
NC_000013.10:g.32954370_32954378delinsGTTGGCAAA , CM000675.1:g.32954370_32954378delinsGTTGGCAAA GRCh37
NC_000013.9:g.31852370_31852378delinsGTTGGCAAA NCBI36
NG_012772.3:g.69754_69762delinsGTTGGCAAA , LRG_293:g.69754_69762delinsGTTGGCAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.9256+88_9256+96delinsGTTGGCAAA ENSP00000434898.2:n.9256+88_9256+96delinsGTTGGCAAA
ENST00000528762.2:c.*623+88_*623+96delinsGTTGGCAAA ENSP00000433168.2:n.*623+88_*623+96delinsGTTGGCAAA
ENST00000530893.7:c.8887+88_8887+96delinsGTTGGCAAA ENSP00000499438.2:n.8887+88_8887+96delinsGTTGGCAAA
ENST00000665585.2:c.*818+88_*818+96delinsGTTGGCAAA ENSP00000499570.2:n.*818+88_*818+96delinsGTTGGCAAA
ENST00000666593.2:c.9256+88_9256+96delinsGTTGGCAAA ENSP00000499256.2:n.9256+88_9256+96delinsGTTGGCAAA
ENST00000700202.2:c.9205+88_9205+96delinsGTTGGCAAA ENSP00000514856.2:n.9205+88_9205+96delinsGTTGGCAAA
ENST00000700202.1:c.1672+88_1672+96delinsGTTGGCAAA ENSP00000514856.1:n.1672+88_1672+96delinsGTTGGCAAA
ENST00000700203.1:n.1383+88_1383+96delinsGTTGGCAAA
ENST00000380152.8:c.9256+88_9256+96delinsGTTGGCAAA MANE Select ENSP00000369497.3:n.9256+88_9256+96delinsGTTGGCAAA
ENST00000544455.6:c.9256+88_9256+96delinsGTTGGCAAA ENSP00000439902.1:n.9256+88_9256+96delinsGTTGGCAAA
ENST00000614259.2:c.9264+88_9264+96delinsGTTGGCAAA ENSP00000506251.1:n.9264+88_9264+96delinsGTTGGCAAA
ENST00000665585.1:c.2134+88_2134+96delinsGTTGGCAAA
ENST00000666593.1:c.139+88_139+96delinsGTTGGCAAA ENSP00000499256.1:n.139+88_139+96delinsGTTGGCAAA
ENST00000680887.1:c.9256+88_9256+96delinsGTTGGCAAA ENSP00000505508.1:n.9256+88_9256+96delinsGTTGGCAAA
ENST00000380152.7:c.9256+88_9256+96delinsGTTGGCAAA ENSP00000369497.3:n.9256+88_9256+96delinsGTTGGCAAA
ENST00000470094.1:c.213+88_213+96delinsGTTGGCAAA
ENST00000544455.5:c.9256+88_9256+96delinsGTTGGCAAA ENSP00000439902.1:n.9256+88_9256+96delinsGTTGGCAAA
NM_000059.3:c.9256+88_9256+96delinsGTTGGCAAA , LRG_293t1:c.9256+88_9256+96delinsGTTGGCAAA NP_000050.2:n.9256+88_9256+96delinsGTTGGCAAA
XM_011535203.1:c.9256+88_9256+96delinsGTTGGCAAA XP_011533505.1:n.9256+88_9256+96delinsGTTGGCAAA
XM_011535204.1:c.9160+88_9160+96delinsGTTGGCAAA XP_011533506.1:n.9160+88_9160+96delinsGTTGGCAAA
NM_000059.4:c.9256+88_9256+96delinsGTTGGCAAA MANE Select NP_000050.3:n.9256+88_9256+96delinsGTTGGCAAA