Canonical Allele Identifier: CA2082816114
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32371042_32371043delinsAC , CM000675.2:g.32371042_32371043delinsAC GRCh38
NC_000013.10:g.32945179_32945180delinsAC , CM000675.1:g.32945179_32945180delinsAC GRCh37
NC_000013.9:g.31843179_31843180delinsAC NCBI36
NG_012772.3:g.60563_60564delinsAC , LRG_293:g.60563_60564delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.8574_8575delinsAC ENSP00000434898.2:p.Gln2858=
ENST00000528762.2:c.8574_8575delinsAC ENSP00000433168.2:p.Gln2858=
ENST00000530893.7:c.8205_8206delinsAC ENSP00000499438.2:p.Gln2735=
ENST00000665585.2:c.8574_8575delinsAC ENSP00000499570.2:p.Gln2858=
ENST00000666593.2:c.8574_8575delinsAC ENSP00000499256.2:p.Gln2858=
ENST00000700202.2:c.8574_8575delinsAC ENSP00000514856.2:p.Gln2858=
ENST00000700202.1:c.1041_1042delinsAC ENSP00000514856.1:p.Gln347=
ENST00000380152.8:c.8574_8575delinsAC MANE Select ENSP00000369497.3:p.Gln2858=
ENST00000544455.6:c.8574_8575delinsAC ENSP00000439902.1:p.Gln2858=
ENST00000614259.2:c.8582_8583delinsAC ENSP00000506251.1:n.8582_8583delinsAC
ENST00000665585.1:c.1139_1140delinsAC
ENST00000680887.1:c.8574_8575delinsAC ENSP00000505508.1:p.Gln2858=
ENST00000380152.7:c.8574_8575delinsAC ENSP00000369497.3:p.Gln2858=
ENST00000528762.1:c.72_73delinsAC ENSP00000433168.1:p.Gln24=
ENST00000544455.5:c.8574_8575delinsAC ENSP00000439902.1:p.Gln2858=
NM_000059.3:c.8574_8575delinsAC , LRG_293t1:c.8574_8575delinsAC NP_000050.2:p.Gln2858=
XM_011535203.1:c.8574_8575delinsAC XP_011533505.1:p.Gln2858=
XM_011535204.1:c.8478_8479delinsAC XP_011533506.1:p.Gln2826=
XM_011535205.1:c.8574_8575delinsAC XP_011533507.1:p.Gln2858=
NM_000059.4:c.8574_8575delinsAC MANE Select NP_000050.3:p.Gln2858=