Canonical Allele Identifier: CA2082758945
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32330932_32330933delinsAT , CM000675.2:g.32330932_32330933delinsAT GRCh38
NC_000013.10:g.32905069_32905070delinsAT , CM000675.1:g.32905069_32905070delinsAT GRCh37
NC_000013.9:g.31803069_31803070delinsAT NCBI36
NG_012772.3:g.20453_20454delinsAT , LRG_293:g.20453_20454delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.695_696delinsAT ENSP00000434898.2:p.Tyr232=
ENST00000528762.2:c.695_696delinsAT ENSP00000433168.2:p.Tyr232=
ENST00000530893.7:c.326_327delinsAT ENSP00000499438.2:p.Tyr109=
ENST00000665585.2:c.695_696delinsAT ENSP00000499570.2:p.Tyr232=
ENST00000666593.2:c.695_696delinsAT ENSP00000499256.2:p.Tyr232=
ENST00000700202.2:c.695_696delinsAT ENSP00000514856.2:p.Tyr232=
ENST00000700201.1:c.*474_*475delinsAT ENSP00000514855.1:n.*474_*475delinsAT
ENST00000380152.8:c.695_696delinsAT MANE Select ENSP00000369497.3:p.Tyr232=
ENST00000544455.6:c.695_696delinsAT ENSP00000439902.1:p.Tyr232=
ENST00000614259.2:c.695_696delinsAT ENSP00000506251.1:p.Tyr232=
ENST00000680887.1:c.695_696delinsAT ENSP00000505508.1:p.Tyr232=
ENST00000380152.7:c.695_696delinsAT ENSP00000369497.3:p.Tyr232=
ENST00000530893.6:n.893_894delinsAT
ENST00000544455.5:c.695_696delinsAT ENSP00000439902.1:p.Tyr232=
ENST00000614259.1:n.695_696delinsAT
NM_000059.3:c.695_696delinsAT , LRG_293t1:c.695_696delinsAT NP_000050.2:p.Tyr232=
XM_011535203.1:c.695_696delinsAT XP_011533505.1:p.Tyr232=
XM_011535204.1:c.695_696delinsAT XP_011533506.1:p.Tyr232=
XM_011535205.1:c.695_696delinsAT XP_011533507.1:p.Tyr232=
NM_000059.4:c.695_696delinsAT MANE Select NP_000050.3:p.Tyr232=