Canonical Allele Identifier: CA2082814931
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32356530_32356531delinsCA , CM000675.2:g.32356530_32356531delinsCA GRCh38
NC_000013.10:g.32930667_32930668delinsCA , CM000675.1:g.32930667_32930668delinsCA GRCh37
NC_000013.9:g.31828667_31828668delinsCA NCBI36
NG_012772.3:g.46051_46052delinsCA , LRG_293:g.46051_46052delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.7538_7539delinsCA ENSP00000434898.2:p.Ala2513=
ENST00000528762.2:c.7538_7539delinsCA ENSP00000433168.2:p.Ala2513=
ENST00000530893.7:c.7169_7170delinsCA ENSP00000499438.2:p.Ala2390=
ENST00000665585.2:c.7538_7539delinsCA ENSP00000499570.2:p.Ala2513=
ENST00000666593.2:c.7538_7539delinsCA ENSP00000499256.2:p.Ala2513=
ENST00000700202.2:c.7538_7539delinsCA ENSP00000514856.2:p.Ala2513=
ENST00000700202.1:c.5_6delinsCA ENSP00000514856.1:p.Ala2=
ENST00000380152.8:c.7538_7539delinsCA MANE Select ENSP00000369497.3:p.Ala2513=
ENST00000544455.6:c.7538_7539delinsCA ENSP00000439902.1:p.Ala2513=
ENST00000614259.2:c.7538_7539delinsCA ENSP00000506251.1:p.Ala2513=
ENST00000665585.1:c.103_104delinsCA
ENST00000680887.1:c.7538_7539delinsCA ENSP00000505508.1:p.Ala2513=
ENST00000380152.7:c.7538_7539delinsCA ENSP00000369497.3:p.Ala2513=
ENST00000544455.5:c.7538_7539delinsCA ENSP00000439902.1:p.Ala2513=
ENST00000614259.1:n.7538_7539delinsCA
NM_000059.3:c.7538_7539delinsCA , LRG_293t1:c.7538_7539delinsCA NP_000050.2:p.Ala2513=
XM_011535203.1:c.7538_7539delinsCA XP_011533505.1:p.Ala2513=
XM_011535204.1:c.7442_7443delinsCA XP_011533506.1:p.Ala2481=
XM_011535205.1:c.7538_7539delinsCA XP_011533507.1:p.Ala2513=
NM_000059.4:c.7538_7539delinsCA MANE Select NP_000050.3:p.Ala2513=