Canonical Allele Identifier: CA2082814971
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32356535_32356536delinsAC , CM000675.2:g.32356535_32356536delinsAC GRCh38
NC_000013.10:g.32930672_32930673delinsAC , CM000675.1:g.32930672_32930673delinsAC GRCh37
NC_000013.9:g.31828672_31828673delinsAC NCBI36
NG_012772.3:g.46056_46057delinsAC , LRG_293:g.46056_46057delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.7543_7544delinsAC ENSP00000434898.2:p.Thr2515=
ENST00000528762.2:c.7543_7544delinsAC ENSP00000433168.2:p.Thr2515=
ENST00000530893.7:c.7174_7175delinsAC ENSP00000499438.2:p.Thr2392=
ENST00000665585.2:c.7543_7544delinsAC ENSP00000499570.2:p.Thr2515=
ENST00000666593.2:c.7543_7544delinsAC ENSP00000499256.2:p.Thr2515=
ENST00000700202.2:c.7543_7544delinsAC ENSP00000514856.2:p.Thr2515=
ENST00000700202.1:c.10_11delinsAC ENSP00000514856.1:p.Thr4=
ENST00000380152.8:c.7543_7544delinsAC MANE Select ENSP00000369497.3:p.Thr2515=
ENST00000544455.6:c.7543_7544delinsAC ENSP00000439902.1:p.Thr2515=
ENST00000614259.2:c.7543_7544delinsAC ENSP00000506251.1:p.Thr2515=
ENST00000665585.1:c.108_109delinsAC
ENST00000680887.1:c.7543_7544delinsAC ENSP00000505508.1:p.Thr2515=
ENST00000380152.7:c.7543_7544delinsAC ENSP00000369497.3:p.Thr2515=
ENST00000544455.5:c.7543_7544delinsAC ENSP00000439902.1:p.Thr2515=
ENST00000614259.1:n.7543_7544delinsAC
NM_000059.3:c.7543_7544delinsAC , LRG_293t1:c.7543_7544delinsAC NP_000050.2:p.Thr2515=
XM_011535203.1:c.7543_7544delinsAC XP_011533505.1:p.Thr2515=
XM_011535204.1:c.7447_7448delinsAC XP_011533506.1:p.Thr2483=
XM_011535205.1:c.7543_7544delinsAC XP_011533507.1:p.Thr2515=
NM_000059.4:c.7543_7544delinsAC MANE Select NP_000050.3:p.Thr2515=