Canonical Allele Identifier: CA022100
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 51844
dbSNP Id: rs397507779

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32339705_32339706delinsT , CM000675.2:g.32339705_32339706delinsT GRCh38
NC_000013.10:g.32913842_32913843delinsT , CM000675.1:g.32913842_32913843delinsT GRCh37
NC_000013.9:g.31811842_31811843delinsT NCBI36
NG_012772.3:g.29226_29227delinsT , LRG_293:g.29226_29227delinsT

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.5350_5351delinsT ENSP00000434898.2:p.Asn1784SerfsTer7
ENST00000528762.2:c.5350_5351delinsT ENSP00000433168.2:p.Asn1784SerfsTer7
ENST00000530893.7:c.4981_4982delinsT ENSP00000499438.2:p.Asn1661SerfsTer7
ENST00000665585.2:c.5350_5351delinsT ENSP00000499570.2:p.Asn1784SerfsTer7
ENST00000666593.2:c.5350_5351delinsT ENSP00000499256.2:p.Asn1784SerfsTer7
ENST00000700202.2:c.5350_5351delinsT ENSP00000514856.2:p.Asn1784SerfsTer7
ENST00000380152.8:c.5350_5351delinsT MANE Select ENSP00000369497.3:p.Asn1784SerfsTer7
ENST00000544455.6:c.5350_5351delinsT ENSP00000439902.1:p.Asn1784SerfsTer7
ENST00000614259.2:c.5350_5351delinsT ENSP00000506251.1:p.Asn1784SerfsTer7
ENST00000680887.1:c.5350_5351delinsT ENSP00000505508.1:p.Asn1784SerfsTer7
ENST00000380152.7:c.5350_5351delinsT ENSP00000369497.3:p.Asn1784SerfsTer7
ENST00000544455.5:c.5350_5351delinsT ENSP00000439902.1:p.Asn1784SerfsTer7
ENST00000614259.1:n.5350_5351delinsT
NM_000059.3:c.5350_5351delinsT , LRG_293t1:c.5350_5351delinsT NP_000050.2:p.Asn1784SerfsTer7
XM_011535203.1:c.5350_5351delinsT XP_011533505.1:p.Asn1784SerfsTer7
XM_011535204.1:c.5350_5351delinsT XP_011533506.1:p.Asn1784SerfsTer7
XM_011535205.1:c.5350_5351delinsT XP_011533507.1:p.Asn1784SerfsTer7
NM_000059.4:c.5350_5351delinsT MANE Select NP_000050.3:p.Asn1784SerfsTer7