Canonical Allele Identifier: CA001794
Gene: BRCA1 HGNC NCBI
BRCA Exchange:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43092803_43092807del , CM000679.2:g.43092803_43092807del GRCh38
NC_000017.10:g.41244820_41244824del , CM000679.1:g.41244820_41244824del GRCh37
NC_000017.9:g.38498346_38498350del NCBI36
NG_005905.2:g.125179_125183del , LRG_292:g.125179_125183del

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.2790_2794del
ENST00000461574.2:c.2726_2730del ENSP00000417241.2:p.Asn909ArgfsTer4
ENST00000470026.6:c.2726_2730del ENSP00000419274.2:p.Asn909ArgfsTer4
ENST00000473961.6:c.2600_2604del ENSP00000420201.2:p.Asn867ArgfsTer4
ENST00000476777.6:c.2723_2727del ENSP00000417554.2:p.Asn908ArgfsTer4
ENST00000477152.6:c.2648_2652del ENSP00000419988.2:p.Asn883ArgfsTer4
ENST00000478531.6:c.785-1773_785-1769del ENSP00000420412.2:n.785-1773_785-1769del
ENST00000489037.2:c.2648_2652del ENSP00000420781.2:p.Asn883ArgfsTer4
ENST00000493919.6:c.647-1773_647-1769del ENSP00000418819.2:n.647-1773_647-1769del
ENST00000494123.6:c.2726_2730del ENSP00000419103.2:p.Asn909ArgfsTer4
ENST00000497488.2:c.1838_1842del ENSP00000418986.2:p.Asn613ArgfsTer4
ENST00000618469.2:c.2726_2730del ENSP00000478114.2:p.Asn909ArgfsTer4
ENST00000634433.2:c.2603_2607del ENSP00000489431.2:p.Asn868ArgfsTer4
ENST00000644379.2:c.2726_2730del ENSP00000496570.2:p.Asn909ArgfsTer4
ENST00000644555.2:c.647-1773_647-1769del ENSP00000494614.2:n.647-1773_647-1769del
ENST00000652672.2:c.2585_2589del ENSP00000498906.2:p.Asn862ArgfsTer4
ENST00000484087.6:c.665-1773_665-1769del ENSP00000419481.2:n.665-1773_665-1769del
ENST00000700182.1:c.707-1773_707-1769del ENSP00000514849.1:n.707-1773_707-1769del
ENST00000357654.9:c.2726_2730del MANE Select ENSP00000350283.3:p.Asn909ArgfsTer4
ENST00000471181.7:c.2726_2730del ENSP00000418960.2:p.Asn909ArgfsTer4
ENST00000352993.7:c.671-1773_671-1769del ENSP00000312236.5:n.671-1773_671-1769del
ENST00000354071.7:c.2726_2730del ENSP00000326002.7:p.Asn909ArgfsTer4
ENST00000357654.7:c.2726_2730del ENSP00000350283.3:p.Asn909ArgfsTer4
ENST00000461221.5:c.*2509_*2513del ENSP00000418548.1:n.*2509_*2513del
ENST00000468300.5:c.788-1773_788-1769del ENSP00000417148.1:n.788-1773_788-1769del
ENST00000471181.6:c.2726_2730del ENSP00000418960.2:p.Asn909ArgfsTer4
ENST00000478531.5:c.785-1773_785-1769del ENSP00000420412.1:n.785-1773_785-1769del
ENST00000484087.5:c.410-1773_410-1769del ENSP00000419481.1:n.410-1773_410-1769del
ENST00000487825.5:c.413-1773_413-1769del ENSP00000418212.1:n.413-1773_413-1769del
ENST00000491747.6:c.788-1773_788-1769del ENSP00000420705.2:n.788-1773_788-1769del
ENST00000493795.5:c.2585_2589del ENSP00000418775.1:p.Asn862ArgfsTer4
ENST00000493919.5:c.647-1773_647-1769del ENSP00000418819.1:n.647-1773_647-1769del
ENST00000586385.5:c.5-28854_5-28850del ENSP00000465818.1:n.5-28854_5-28850del
ENST00000591534.5:c.-43-18284_-43-18280del ENSP00000467329.1:n.-43-18284_-43-18280del
ENST00000591849.5:c.-99+32466_-99+32470del ENSP00000465347.1:n.-99+32466_-99+32470del
NM_007294.3:c.2726_2730del , LRG_292t1:c.2726_2730del NP_009225.1:p.Asn909ArgfsTer4
NM_007297.3:c.2585_2589del NP_009228.2:p.Asn862ArgfsTer4
NM_007298.3:c.788-1773_788-1769del NP_009229.2:n.788-1773_788-1769del
NM_007299.3:c.788-1773_788-1769del NP_009230.2:n.788-1773_788-1769del
NM_007300.3:c.2726_2730del NP_009231.2:p.Asn909ArgfsTer4
NR_027676.1:n.2862_2866del
NM_007294.4:c.2726_2730del MANE Select NP_009225.1:p.Asn909ArgfsTer4
NM_007297.4:c.2585_2589del NP_009228.2:p.Asn862ArgfsTer4
NM_007299.4:c.788-1773_788-1769del NP_009230.2:n.788-1773_788-1769del
NM_007300.4:c.2726_2730del NP_009231.2:p.Asn909ArgfsTer4
NR_027676.2:n.2903_2907del