Canonical Allele Identifier: CA2082819233
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32357935_32357937delinsCTA , CM000675.2:g.32357935_32357937delinsCTA GRCh38
NC_000013.10:g.32932072_32932074delinsCTA , CM000675.1:g.32932072_32932074delinsCTA GRCh37
NC_000013.9:g.31830072_31830074delinsCTA NCBI36
NG_012772.3:g.47456_47458delinsCTA , LRG_293:g.47456_47458delinsCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.7805+6_7805+8delinsCTA ENSP00000434898.2:n.7805+6_7805+8delinsCTA
ENST00000528762.2:c.7805+6_7805+8delinsCTA ENSP00000433168.2:n.7805+6_7805+8delinsCTA
ENST00000530893.7:c.7436+6_7436+8delinsCTA ENSP00000499438.2:n.7436+6_7436+8delinsCTA
ENST00000665585.2:c.7805+6_7805+8delinsCTA ENSP00000499570.2:n.7805+6_7805+8delinsCTA
ENST00000666593.2:c.7805+6_7805+8delinsCTA ENSP00000499256.2:n.7805+6_7805+8delinsCTA
ENST00000700202.2:c.7805+6_7805+8delinsCTA ENSP00000514856.2:n.7805+6_7805+8delinsCTA
ENST00000700202.1:c.272+6_272+8delinsCTA ENSP00000514856.1:n.272+6_272+8delinsCTA
ENST00000380152.8:c.7805+6_7805+8delinsCTA MANE Select ENSP00000369497.3:n.7805+6_7805+8delinsCTA
ENST00000544455.6:c.7805+6_7805+8delinsCTA ENSP00000439902.1:n.7805+6_7805+8delinsCTA
ENST00000614259.2:c.7805+6_7805+8delinsCTA ENSP00000506251.1:n.7805+6_7805+8delinsCTA
ENST00000665585.1:c.370+6_370+8delinsCTA
ENST00000680887.1:c.7805+6_7805+8delinsCTA ENSP00000505508.1:n.7805+6_7805+8delinsCTA
ENST00000380152.7:c.7805+6_7805+8delinsCTA ENSP00000369497.3:n.7805+6_7805+8delinsCTA
ENST00000544455.5:c.7805+6_7805+8delinsCTA ENSP00000439902.1:n.7805+6_7805+8delinsCTA
ENST00000614259.1:n.7805+6_7805+8delinsCTA
NM_000059.3:c.7805+6_7805+8delinsCTA , LRG_293t1:c.7805+6_7805+8delinsCTA NP_000050.2:n.7805+6_7805+8delinsCTA
XM_011535203.1:c.7805+6_7805+8delinsCTA XP_011533505.1:n.7805+6_7805+8delinsCTA
XM_011535204.1:c.7709+6_7709+8delinsCTA XP_011533506.1:n.7709+6_7709+8delinsCTA
XM_011535205.1:c.7805+6_7805+8delinsCTA XP_011533507.1:n.7805+6_7805+8delinsCTA
NM_000059.4:c.7805+6_7805+8delinsCTA MANE Select NP_000050.3:n.7805+6_7805+8delinsCTA