Canonical Allele Identifier: CA16619630
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 421345
dbSNP Id: rs1064795074

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32316435_32316436delinsAG , CM000675.2:g.32316435_32316436delinsAG GRCh38
NC_000013.10:g.32890572_32890573delinsAG , CM000675.1:g.32890572_32890573delinsAG GRCh37
NC_000013.9:g.31788572_31788573delinsAG NCBI36
NG_012772.3:g.5956_5957delinsAG , LRG_293:g.5956_5957delinsAG
NG_017006.1:g.519_520delinsCT
NG_017006.2:g.3928_3929delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.-26_-25delinsAG ENSP00000434898.2:n.-26_-25delinsAG
ENST00000528762.2:c.-26_-25delinsAG ENSP00000433168.2:n.-26_-25delinsAG
ENST00000530893.7:c.-391_-390delinsAG ENSP00000499438.2:n.-391_-390delinsAG
ENST00000665585.2:c.-26_-25delinsAG ENSP00000499570.2:n.-26_-25delinsAG
ENST00000666593.2:c.-26_-25delinsAG ENSP00000499256.2:n.-26_-25delinsAG
ENST00000700202.2:c.-26_-25delinsAG ENSP00000514856.2:n.-26_-25delinsAG
ENST00000700199.1:n.99_100delinsAG
ENST00000700200.1:n.99_100delinsAG
ENST00000700201.1:c.-26_-25delinsAG ENSP00000514855.1:n.-26_-25delinsAG
ENST00000380152.8:c.-26_-25delinsAG MANE Select ENSP00000369497.3:n.-26_-25delinsAG
ENST00000544455.6:c.-26_-25delinsAG ENSP00000439902.1:n.-26_-25delinsAG
ENST00000680887.1:c.-26_-25delinsAG ENSP00000505508.1:n.-26_-25delinsAG
ENST00000380152.7:c.-26_-25delinsAG ENSP00000369497.3:n.-26_-25delinsAG
ENST00000530893.6:n.177_178delinsAG
ENST00000544455.5:c.-26_-25delinsAG ENSP00000439902.1:n.-26_-25delinsAG
NM_000059.3:c.-26_-25delinsAG , LRG_293t1:c.-26_-25delinsAG NP_000050.2:n.-26_-25delinsAG
XM_011535203.1:c.-26_-25delinsAG XP_011533505.1:n.-26_-25delinsAG
XM_011535204.1:c.-26_-25delinsAG XP_011533506.1:n.-26_-25delinsAG
XM_011535205.1:c.-26_-25delinsAG XP_011533507.1:n.-26_-25delinsAG
NM_000059.4:c.-26_-25delinsAG MANE Select NP_000050.3:n.-26_-25delinsAG