Canonical Allele Identifier: CA2082760023
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32331127_32331128delinsCG , CM000675.2:g.32331127_32331128delinsCG GRCh38
NC_000013.10:g.32905264_32905265delinsCG , CM000675.1:g.32905264_32905265delinsCG GRCh37
NC_000013.9:g.31803264_31803265delinsCG NCBI36
NG_012772.3:g.20648_20649delinsCG , LRG_293:g.20648_20649delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.793+97_793+98delinsCG ENSP00000434898.2:n.793+97_793+98delinsCG
ENST00000528762.2:c.793+97_793+98delinsCG ENSP00000433168.2:n.793+97_793+98delinsCG
ENST00000530893.7:c.424+97_424+98delinsCG ENSP00000499438.2:n.424+97_424+98delinsCG
ENST00000665585.2:c.793+97_793+98delinsCG ENSP00000499570.2:n.793+97_793+98delinsCG
ENST00000666593.2:c.793+97_793+98delinsCG ENSP00000499256.2:n.793+97_793+98delinsCG
ENST00000700202.2:c.793+97_793+98delinsCG ENSP00000514856.2:n.793+97_793+98delinsCG
ENST00000700201.1:c.*572+97_*572+98delinsCG ENSP00000514855.1:n.*572+97_*572+98delinsCG
ENST00000380152.8:c.793+97_793+98delinsCG MANE Select ENSP00000369497.3:n.793+97_793+98delinsCG
ENST00000544455.6:c.793+97_793+98delinsCG ENSP00000439902.1:n.793+97_793+98delinsCG
ENST00000614259.2:c.793+97_793+98delinsCG ENSP00000506251.1:n.793+97_793+98delinsCG
ENST00000680887.1:c.793+97_793+98delinsCG ENSP00000505508.1:n.793+97_793+98delinsCG
ENST00000380152.7:c.793+97_793+98delinsCG ENSP00000369497.3:n.793+97_793+98delinsCG
ENST00000530893.6:n.991+97_991+98delinsCG
ENST00000544455.5:c.793+97_793+98delinsCG ENSP00000439902.1:n.793+97_793+98delinsCG
ENST00000614259.1:n.793+97_793+98delinsCG
NM_000059.3:c.793+97_793+98delinsCG , LRG_293t1:c.793+97_793+98delinsCG NP_000050.2:n.793+97_793+98delinsCG
XM_011535203.1:c.793+97_793+98delinsCG XP_011533505.1:n.793+97_793+98delinsCG
XM_011535204.1:c.793+97_793+98delinsCG XP_011533506.1:n.793+97_793+98delinsCG
XM_011535205.1:c.793+97_793+98delinsCG XP_011533507.1:n.793+97_793+98delinsCG
NM_000059.4:c.793+97_793+98delinsCG MANE Select NP_000050.3:n.793+97_793+98delinsCG