Canonical Allele Identifier: CA2741310335
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32399171_32399172insCCCCTCTTTTT , CM000675.2:g.32399171_32399172insCCCCTCTTTTT GRCh38
NC_000013.10:g.32973308_32973309insCCCCTCTTTTT , CM000675.1:g.32973308_32973309insCCCCTCTTTTT GRCh37
NC_000013.9:g.31871308_31871309insCCCCTCTTTTT NCBI36
NG_012772.3:g.88692_88693insCCCCTCTTTTT , LRG_293:g.88692_88693insCCCCTCTTTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.*1181_*1182insCCCCTCTTTTT ENSP00000434898.2:n.*1181_*1182insCCCCTCTTTTT
ENST00000530893.7:c.*401_*402insCCCCTCTTTTT ENSP00000499438.2:n.*401_*402insCCCCTCTTTTT
ENST00000380152.8:c.*401_*402insCCCCTCTTTTT MANE Select ENSP00000369497.3:n.*401_*402insCCCCTCTTTTT
ENST00000544455.6:c.*401_*402insCCCCTCTTTTT ENSP00000439902.1:n.*401_*402insCCCCTCTTTTT
ENST00000614259.2:c.10666_10667insCCCCTCTTTTT ENSP00000506251.1:n.10666_10667insCCCCTCTTTTT
ENST00000680887.1:c.*401_*402insCCCCTCTTTTT ENSP00000505508.1:n.*401_*402insCCCCTCTTTTT
ENST00000380152.7:c.*401_*402insCCCCTCTTTTT ENSP00000369497.3:n.*401_*402insCCCCTCTTTTT
ENST00000544455.5:c.*401_*402insCCCCTCTTTTT ENSP00000439902.1:n.*401_*402insCCCCTCTTTTT
NM_000059.3:c.*401_*402insCCCCTCTTTTT , LRG_293t1:c.*401_*402insCCCCTCTTTTT NP_000050.2:n.*401_*402insCCCCTCTTTTT
XM_011535203.1:c.*401_*402insCCCCTCTTTTT XP_011533505.1:n.*401_*402insCCCCTCTTTTT
XM_011535204.1:c.*401_*402insCCCCTCTTTTT XP_011533506.1:n.*401_*402insCCCCTCTTTTT
NM_000059.4:c.*401_*402insCCCCTCTTTTT MANE Select NP_000050.3:n.*401_*402insCCCCTCTTTTT