Canonical Allele Identifier: CA2082815189
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32356553_32356557delinsATCTC , CM000675.2:g.32356553_32356557delinsATCTC GRCh38
NC_000013.10:g.32930690_32930694delinsATCTC , CM000675.1:g.32930690_32930694delinsATCTC GRCh37
NC_000013.9:g.31828690_31828694delinsATCTC NCBI36
NG_012772.3:g.46074_46078delinsATCTC , LRG_293:g.46074_46078delinsATCTC

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.7561_7565delinsATCTC ENSP00000434898.2:p.Ile2521=
ENST00000528762.2:c.7561_7565delinsATCTC ENSP00000433168.2:p.Ile2521=
ENST00000530893.7:c.7192_7196delinsATCTC ENSP00000499438.2:p.Ile2398=
ENST00000665585.2:c.7561_7565delinsATCTC ENSP00000499570.2:p.Ile2521=
ENST00000666593.2:c.7561_7565delinsATCTC ENSP00000499256.2:p.Ile2521=
ENST00000700202.2:c.7561_7565delinsATCTC ENSP00000514856.2:p.Ile2521=
ENST00000700202.1:c.28_32delinsATCTC ENSP00000514856.1:p.Ile10=
ENST00000380152.8:c.7561_7565delinsATCTC MANE Select ENSP00000369497.3:p.Ile2521=
ENST00000544455.6:c.7561_7565delinsATCTC ENSP00000439902.1:p.Ile2521=
ENST00000614259.2:c.7561_7565delinsATCTC ENSP00000506251.1:p.Ile2521=
ENST00000665585.1:c.126_130delinsATCTC
ENST00000680887.1:c.7561_7565delinsATCTC ENSP00000505508.1:p.Ile2521=
ENST00000380152.7:c.7561_7565delinsATCTC ENSP00000369497.3:p.Ile2521=
ENST00000544455.5:c.7561_7565delinsATCTC ENSP00000439902.1:p.Ile2521=
ENST00000614259.1:n.7561_7565delinsATCTC
NM_000059.3:c.7561_7565delinsATCTC , LRG_293t1:c.7561_7565delinsATCTC NP_000050.2:p.Ile2521=
XM_011535203.1:c.7561_7565delinsATCTC XP_011533505.1:p.Ile2521=
XM_011535204.1:c.7465_7469delinsATCTC XP_011533506.1:p.Ile2489=
XM_011535205.1:c.7561_7565delinsATCTC XP_011533507.1:p.Ile2521=
NM_000059.4:c.7561_7565delinsATCTC MANE Select NP_000050.3:p.Ile2521=