Canonical Allele Identifier: CA2082775117
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32316406_32316409delinsGTCT , CM000675.2:g.32316406_32316409delinsGTCT GRCh38
NC_000013.10:g.32890543_32890546delinsGTCT , CM000675.1:g.32890543_32890546delinsGTCT GRCh37
NC_000013.9:g.31788543_31788546delinsGTCT NCBI36
NG_012772.3:g.5927_5930delinsGTCT , LRG_293:g.5927_5930delinsGTCT
NG_017006.1:g.546_549delinsAGAC
NG_017006.2:g.3955_3958delinsAGAC

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.-39-16_-39-13delinsGTCT ENSP00000434898.2:n.-39-16_-39-13delinsGT...
ENST00000528762.2:c.-39-16_-39-13delinsGTCT ENSP00000433168.2:n.-39-16_-39-13delinsGT...
ENST00000530893.7:c.-404-16_-404-13delinsGTCT ENSP00000499438.2:n.-404-16_-404-13delins...
ENST00000665585.2:c.-39-16_-39-13delinsGTCT ENSP00000499570.2:n.-39-16_-39-13delinsGT...
ENST00000666593.2:c.-39-16_-39-13delinsGTCT ENSP00000499256.2:n.-39-16_-39-13delinsGT...
ENST00000700202.2:c.-39-16_-39-13delinsGTCT ENSP00000514856.2:n.-39-16_-39-13delinsGT...
ENST00000700199.1:n.86-16_86-13delinsGTCT
ENST00000700200.1:n.86-16_86-13delinsGTCT
ENST00000700201.1:c.-39-16_-39-13delinsGTCT ENSP00000514855.1:n.-39-16_-39-13delinsGT...
ENST00000380152.8:c.-39-16_-39-13delinsGTCT MANE Select ENSP00000369497.3:n.-39-16_-39-13delinsGT...
ENST00000544455.6:c.-39-16_-39-13delinsGTCT ENSP00000439902.1:n.-39-16_-39-13delinsGT...
ENST00000680887.1:c.-39-16_-39-13delinsGTCT ENSP00000505508.1:n.-39-16_-39-13delinsGT...
ENST00000380152.7:c.-39-16_-39-13delinsGTCT ENSP00000369497.3:n.-39-16_-39-13delinsGT...
ENST00000530893.6:n.164-16_164-13delinsGTCT
ENST00000544455.5:c.-39-16_-39-13delinsGTCT ENSP00000439902.1:n.-39-16_-39-13delinsGT...
NM_000059.3:c.-39-16_-39-13delinsGTCT , LRG_293t1:c.-39-16_-39-13delinsGTCT NP_000050.2:n.-39-16_-39-13delinsGTCT
XM_011535203.1:c.-39-16_-39-13delinsGTCT XP_011533505.1:n.-39-16_-39-13delinsGTCT
XM_011535204.1:c.-39-16_-39-13delinsGTCT XP_011533506.1:n.-39-16_-39-13delinsGTCT
XM_011535205.1:c.-39-16_-39-13delinsGTCT XP_011533507.1:n.-39-16_-39-13delinsGTCT
NM_000059.4:c.-39-16_-39-13delinsGTCT MANE Select NP_000050.3:n.-39-16_-39-13delinsGTCT