Canonical Allele Identifier: CA2082814921
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32356529_32356530delinsGC , CM000675.2:g.32356529_32356530delinsGC GRCh38
NC_000013.10:g.32930666_32930667delinsGC , CM000675.1:g.32930666_32930667delinsGC GRCh37
NC_000013.9:g.31828666_31828667delinsGC NCBI36
NG_012772.3:g.46050_46051delinsGC , LRG_293:g.46050_46051delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.7537_7538delinsGC ENSP00000434898.2:p.Ala2513=
ENST00000528762.2:c.7537_7538delinsGC ENSP00000433168.2:p.Ala2513=
ENST00000530893.7:c.7168_7169delinsGC ENSP00000499438.2:p.Ala2390=
ENST00000665585.2:c.7537_7538delinsGC ENSP00000499570.2:p.Ala2513=
ENST00000666593.2:c.7537_7538delinsGC ENSP00000499256.2:p.Ala2513=
ENST00000700202.2:c.7537_7538delinsGC ENSP00000514856.2:p.Ala2513=
ENST00000700202.1:c.4_5delinsGC ENSP00000514856.1:p.Ala2=
ENST00000380152.8:c.7537_7538delinsGC MANE Select ENSP00000369497.3:p.Ala2513=
ENST00000544455.6:c.7537_7538delinsGC ENSP00000439902.1:p.Ala2513=
ENST00000614259.2:c.7537_7538delinsGC ENSP00000506251.1:p.Ala2513=
ENST00000665585.1:c.102_103delinsGC
ENST00000680887.1:c.7537_7538delinsGC ENSP00000505508.1:p.Ala2513=
ENST00000380152.7:c.7537_7538delinsGC ENSP00000369497.3:p.Ala2513=
ENST00000544455.5:c.7537_7538delinsGC ENSP00000439902.1:p.Ala2513=
ENST00000614259.1:n.7537_7538delinsGC
NM_000059.3:c.7537_7538delinsGC , LRG_293t1:c.7537_7538delinsGC NP_000050.2:p.Ala2513=
XM_011535203.1:c.7537_7538delinsGC XP_011533505.1:p.Ala2513=
XM_011535204.1:c.7441_7442delinsGC XP_011533506.1:p.Ala2481=
XM_011535205.1:c.7537_7538delinsGC XP_011533507.1:p.Ala2513=
NM_000059.4:c.7537_7538delinsGC MANE Select NP_000050.3:p.Ala2513=