Canonical Allele Identifier: CA2082815314
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32356569_32356571delinsCAG , CM000675.2:g.32356569_32356571delinsCAG GRCh38
NC_000013.10:g.32930706_32930708delinsCAG , CM000675.1:g.32930706_32930708delinsCAG GRCh37
NC_000013.9:g.31828706_31828708delinsCAG NCBI36
NG_012772.3:g.46090_46092delinsCAG , LRG_293:g.46090_46092delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.7577_7579delinsCAG ENSP00000434898.2:p.Ala2526=
ENST00000528762.2:c.7577_7579delinsCAG ENSP00000433168.2:p.Ala2526=
ENST00000530893.7:c.7208_7210delinsCAG ENSP00000499438.2:p.Ala2403=
ENST00000665585.2:c.7577_7579delinsCAG ENSP00000499570.2:p.Ala2526=
ENST00000666593.2:c.7577_7579delinsCAG ENSP00000499256.2:p.Ala2526=
ENST00000700202.2:c.7577_7579delinsCAG ENSP00000514856.2:p.Ala2526=
ENST00000700202.1:c.44_46delinsCAG ENSP00000514856.1:p.Ala15=
ENST00000380152.8:c.7577_7579delinsCAG MANE Select ENSP00000369497.3:p.Ala2526=
ENST00000544455.6:c.7577_7579delinsCAG ENSP00000439902.1:p.Ala2526=
ENST00000614259.2:c.7577_7579delinsCAG ENSP00000506251.1:p.Ala2526=
ENST00000665585.1:c.142_144delinsCAG
ENST00000680887.1:c.7577_7579delinsCAG ENSP00000505508.1:p.Ala2526=
ENST00000380152.7:c.7577_7579delinsCAG ENSP00000369497.3:p.Ala2526=
ENST00000544455.5:c.7577_7579delinsCAG ENSP00000439902.1:p.Ala2526=
ENST00000614259.1:n.7577_7579delinsCAG
NM_000059.3:c.7577_7579delinsCAG , LRG_293t1:c.7577_7579delinsCAG NP_000050.2:p.Ala2526=
XM_011535203.1:c.7577_7579delinsCAG XP_011533505.1:p.Ala2526=
XM_011535204.1:c.7481_7483delinsCAG XP_011533506.1:p.Ala2494=
XM_011535205.1:c.7577_7579delinsCAG XP_011533507.1:p.Ala2526=
NM_000059.4:c.7577_7579delinsCAG MANE Select NP_000050.3:p.Ala2526=