Canonical Allele Identifier: CA2499222137
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32337955_32337956insTT , CM000675.2:g.32337955_32337956insTT GRCh38
NC_000013.10:g.32912092_32912093insTT , CM000675.1:g.32912092_32912093insTT GRCh37
NC_000013.9:g.31810092_31810093insTT NCBI36
NG_012772.3:g.27476_27477insTT , LRG_293:g.27476_27477insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.3600_3601insTT ENSP00000434898.2:p.Asn1201LeufsTer9
ENST00000528762.2:c.3600_3601insTT ENSP00000433168.2:p.Asn1201LeufsTer9
ENST00000530893.7:c.3231_3232insTT ENSP00000499438.2:p.Asn1078LeufsTer9
ENST00000665585.2:c.3600_3601insTT ENSP00000499570.2:p.Asn1201LeufsTer9
ENST00000666593.2:c.3600_3601insTT ENSP00000499256.2:p.Asn1201LeufsTer9
ENST00000700202.2:c.3600_3601insTT ENSP00000514856.2:p.Asn1201LeufsTer9
ENST00000380152.8:c.3600_3601insTT MANE Select ENSP00000369497.3:p.Asn1201LeufsTer9
ENST00000544455.6:c.3600_3601insTT ENSP00000439902.1:p.Asn1201LeufsTer9
ENST00000614259.2:c.3600_3601insTT ENSP00000506251.1:p.Asn1201LeufsTer9
ENST00000680887.1:c.3600_3601insTT ENSP00000505508.1:p.Asn1201LeufsTer9
ENST00000380152.7:c.3600_3601insTT ENSP00000369497.3:p.Asn1201LeufsTer9
ENST00000544455.5:c.3600_3601insTT ENSP00000439902.1:p.Asn1201LeufsTer9
ENST00000614259.1:n.3600_3601insTT
NM_000059.3:c.3600_3601insTT , LRG_293t1:c.3600_3601insTT NP_000050.2:p.Asn1201LeufsTer9
XM_011535203.1:c.3600_3601insTT XP_011533505.1:p.Asn1201LeufsTer9
XM_011535204.1:c.3600_3601insTT XP_011533506.1:p.Asn1201LeufsTer9
XM_011535205.1:c.3600_3601insTT XP_011533507.1:p.Asn1201LeufsTer9
NM_000059.4:c.3600_3601insTT MANE Select NP_000050.3:p.Asn1201LeufsTer9