Canonical Allele Identifier: CA16619634
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 423011
dbSNP Id: rs1064796163

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32319069_32319070delinsAA , CM000675.2:g.32319069_32319070delinsAA GRCh38
NC_000013.10:g.32893206_32893207delinsAA , CM000675.1:g.32893206_32893207delinsAA GRCh37
NC_000013.9:g.31791206_31791207delinsAA NCBI36
NG_012772.3:g.8590_8591delinsAA , LRG_293:g.8590_8591delinsAA
NG_017006.2:g.1294_1295delinsTT

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.68-8_68-7delinsAA ENSP00000434898.2:n.68-8_68-7delinsAA
ENST00000528762.2:c.68-8_68-7delinsAA ENSP00000433168.2:n.68-8_68-7delinsAA
ENST00000530893.7:c.-302-8_-302-7delinsAA ENSP00000499438.2:n.-302-8_-302-7delinsAA...
ENST00000665585.2:c.68-8_68-7delinsAA ENSP00000499570.2:n.68-8_68-7delinsAA
ENST00000666593.2:c.68-8_68-7delinsAA ENSP00000499256.2:n.68-8_68-7delinsAA
ENST00000700202.2:c.68-8_68-7delinsAA ENSP00000514856.2:n.68-8_68-7delinsAA
ENST00000700200.1:n.191+2542_191+2543delinsAA
ENST00000700201.1:c.68-8_68-7delinsAA ENSP00000514855.1:n.68-8_68-7delinsAA
ENST00000380152.8:c.68-8_68-7delinsAA MANE Select ENSP00000369497.3:n.68-8_68-7delinsAA
ENST00000544455.6:c.68-8_68-7delinsAA ENSP00000439902.1:n.68-8_68-7delinsAA
ENST00000614259.2:c.68-8_68-7delinsAA ENSP00000506251.1:n.68-8_68-7delinsAA
ENST00000680887.1:c.68-8_68-7delinsAA ENSP00000505508.1:n.68-8_68-7delinsAA
ENST00000380152.7:c.68-8_68-7delinsAA ENSP00000369497.3:n.68-8_68-7delinsAA
ENST00000530893.6:n.266-8_266-7delinsAA
ENST00000544455.5:c.68-8_68-7delinsAA ENSP00000439902.1:n.68-8_68-7delinsAA
ENST00000614259.1:n.68-8_68-7delinsAA
NM_000059.3:c.68-8_68-7delinsAA , LRG_293t1:c.68-8_68-7delinsAA NP_000050.2:n.68-8_68-7delinsAA
XM_011535203.1:c.68-8_68-7delinsAA XP_011533505.1:n.68-8_68-7delinsAA
XM_011535204.1:c.68-8_68-7delinsAA XP_011533506.1:n.68-8_68-7delinsAA
XM_011535205.1:c.68-8_68-7delinsAA XP_011533507.1:n.68-8_68-7delinsAA
NM_000059.4:c.68-8_68-7delinsAA MANE Select NP_000050.3:n.68-8_68-7delinsAA