Canonical Allele Identifier: CA2082817628
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32357757_32357767delinsGTTTCTAAACA , CM000675.2:g.32357757_32357767delinsGTTTCTAAACA GRCh38
NC_000013.10:g.32931894_32931904delinsGTTTCTAAACA , CM000675.1:g.32931894_32931904delinsGTTTCTAAACA GRCh37
NC_000013.9:g.31829894_31829904delinsGTTTCTAAACA NCBI36
NG_012772.3:g.47278_47288delinsGTTTCTAAACA , LRG_293:g.47278_47288delinsGTTTCTAAACA

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.7633_7643delinsGTTTCTAAACA ENSP00000434898.2:p.Val2545=
ENST00000528762.2:c.7633_7643delinsGTTTCTAAACA ENSP00000433168.2:p.Val2545=
ENST00000530893.7:c.7264_7274delinsGTTTCTAAACA ENSP00000499438.2:p.Val2422=
ENST00000665585.2:c.7633_7643delinsGTTTCTAAACA ENSP00000499570.2:p.Val2545=
ENST00000666593.2:c.7633_7643delinsGTTTCTAAACA ENSP00000499256.2:p.Val2545=
ENST00000700202.2:c.7633_7643delinsGTTTCTAAACA ENSP00000514856.2:p.Val2545=
ENST00000700202.1:c.100_110delinsGTTTCTAAACA ENSP00000514856.1:p.Val34=
ENST00000380152.8:c.7633_7643delinsGTTTCTAAACA MANE Select ENSP00000369497.3:p.Val2545=
ENST00000544455.6:c.7633_7643delinsGTTTCTAAACA ENSP00000439902.1:p.Val2545=
ENST00000614259.2:c.7633_7643delinsGTTTCTAAACA ENSP00000506251.1:p.Val2545=
ENST00000665585.1:c.198_208delinsGTTTCTAAACA
ENST00000680887.1:c.7633_7643delinsGTTTCTAAACA ENSP00000505508.1:p.Val2545=
ENST00000380152.7:c.7633_7643delinsGTTTCTAAACA ENSP00000369497.3:p.Val2545=
ENST00000544455.5:c.7633_7643delinsGTTTCTAAACA ENSP00000439902.1:p.Val2545=
ENST00000614259.1:n.7633_7643delinsGTTTCTAAACA
NM_000059.3:c.7633_7643delinsGTTTCTAAACA , LRG_293t1:c.7633_7643delinsGTTTCTAAACA NP_000050.2:p.Val2545=
XM_011535203.1:c.7633_7643delinsGTTTCTAAACA XP_011533505.1:p.Val2545=
XM_011535204.1:c.7537_7547delinsGTTTCTAAACA XP_011533506.1:p.Val2513=
XM_011535205.1:c.7633_7643delinsGTTTCTAAACA XP_011533507.1:p.Val2545=
NM_000059.4:c.7633_7643delinsGTTTCTAAACA MANE Select NP_000050.3:p.Val2545=