Canonical Allele Identifier: CA2082826799
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32376170_32376172delinsACT , CM000675.2:g.32376170_32376172delinsACT GRCh38
NC_000013.10:g.32950307_32950309delinsACT , CM000675.1:g.32950307_32950309delinsACT GRCh37
NC_000013.9:g.31848307_31848309delinsACT NCBI36
NG_012772.3:g.65691_65693delinsACT , LRG_293:g.65691_65693delinsACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.8633-500_8633-498delinsACT ENSP00000434898.2:n.8633-500_8633-498delinsACT
ENST00000528762.2:c.8697-500_8697-498delinsACT ENSP00000433168.2:n.8697-500_8697-498delinsACT
ENST00000530893.7:c.8264-500_8264-498delinsACT ENSP00000499438.2:n.8264-500_8264-498delinsACT
ENST00000665585.2:c.*195-500_*195-498delinsACT ENSP00000499570.2:n.*195-500_*195-498delinsACT
ENST00000666593.2:c.8633-500_8633-498delinsACT ENSP00000499256.2:n.8633-500_8633-498delinsACT
ENST00000700202.2:c.8633-500_8633-498delinsACT ENSP00000514856.2:n.8633-500_8633-498delinsACT
ENST00000700202.1:c.1100-500_1100-498delinsACT ENSP00000514856.1:n.1100-500_1100-498delinsACT
ENST00000700203.1:n.260_262delinsACT
ENST00000380152.8:c.8633-500_8633-498delinsACT MANE Select ENSP00000369497.3:n.8633-500_8633-498delinsACT
ENST00000544455.6:c.8633-500_8633-498delinsACT ENSP00000439902.1:n.8633-500_8633-498delinsACT
ENST00000614259.2:c.8641-500_8641-498delinsACT ENSP00000506251.1:n.8641-500_8641-498delinsACT
ENST00000665585.1:c.1511-500_1511-498delinsACT
ENST00000680887.1:c.8633-500_8633-498delinsACT ENSP00000505508.1:n.8633-500_8633-498delinsACT
ENST00000380152.7:c.8633-500_8633-498delinsACT ENSP00000369497.3:n.8633-500_8633-498delinsACT
ENST00000528762.1:c.195-500_195-498delinsACT ENSP00000433168.1:n.195-500_195-498delinsACT
ENST00000544455.5:c.8633-500_8633-498delinsACT ENSP00000439902.1:n.8633-500_8633-498delinsACT
NM_000059.3:c.8633-500_8633-498delinsACT , LRG_293t1:c.8633-500_8633-498delinsACT NP_000050.2:n.8633-500_8633-498delinsACT
XM_011535203.1:c.8633-500_8633-498delinsACT XP_011533505.1:n.8633-500_8633-498delinsACT
XM_011535204.1:c.8537-500_8537-498delinsACT XP_011533506.1:n.8537-500_8537-498delinsACT
XM_011535205.1:c.8633-500_8633-498delinsACT XP_011533507.1:n.8633-500_8633-498delinsACT
NM_000059.4:c.8633-500_8633-498delinsACT MANE Select NP_000050.3:n.8633-500_8633-498delinsACT