Canonical Allele Identifier: CA2695225996
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43093185_43093204dup , CM000679.2:g.43093185_43093204dup GRCh38
NC_000017.10:g.41245202_41245221dup , CM000679.1:g.41245202_41245221dup GRCh37
NC_000017.9:g.38498728_38498747dup NCBI36
NG_005905.2:g.124782_124801dup , LRG_292:g.124782_124801dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.2393_2412dup
ENST00000461574.2:c.2329_2348dup ENSP00000417241.2:p.Ser784MetfsTer15
ENST00000470026.6:c.2329_2348dup ENSP00000419274.2:p.Ser784MetfsTer15
ENST00000473961.6:c.2203_2222dup ENSP00000420201.2:p.Ser742MetfsTer15
ENST00000476777.6:c.2326_2345dup ENSP00000417554.2:p.Ser783MetfsTer15
ENST00000477152.6:c.2251_2270dup ENSP00000419988.2:p.Ser758MetfsTer15
ENST00000478531.6:c.784+1542_784+1561dup ENSP00000420412.2:n.784+1542_784+1561dup
ENST00000489037.2:c.2251_2270dup ENSP00000420781.2:p.Ser758MetfsTer15
ENST00000493919.6:c.646+1542_646+1561dup ENSP00000418819.2:n.646+1542_646+1561dup
ENST00000494123.6:c.2329_2348dup ENSP00000419103.2:p.Ser784MetfsTer15
ENST00000497488.2:c.1441_1460dup ENSP00000418986.2:p.Ser488MetfsTer15
ENST00000618469.2:c.2329_2348dup ENSP00000478114.2:p.Ser784MetfsTer15
ENST00000634433.2:c.2206_2225dup ENSP00000489431.2:p.Ser743MetfsTer15
ENST00000644379.2:c.2329_2348dup ENSP00000496570.2:p.Ser784MetfsTer15
ENST00000644555.2:c.646+1542_646+1561dup ENSP00000494614.2:n.646+1542_646+1561dup
ENST00000652672.2:c.2188_2207dup ENSP00000498906.2:p.Ser737MetfsTer15
ENST00000484087.6:c.664+1542_664+1561dup ENSP00000419481.2:n.664+1542_664+1561dup
ENST00000700182.1:c.706+1542_706+1561dup ENSP00000514849.1:n.706+1542_706+1561dup
ENST00000357654.9:c.2329_2348dup MANE Select ENSP00000350283.3:p.Ser784MetfsTer15
ENST00000471181.7:c.2329_2348dup ENSP00000418960.2:p.Ser784MetfsTer15
ENST00000352993.7:c.671-2170_671-2151dup ENSP00000312236.5:n.671-2170_671-2151dup
ENST00000354071.7:c.2329_2348dup ENSP00000326002.7:p.Ser784MetfsTer15
ENST00000357654.7:c.2329_2348dup ENSP00000350283.3:p.Ser784MetfsTer15
ENST00000461221.5:c.*2112_*2131dup ENSP00000418548.1:n.*2112_*2131dup
ENST00000468300.5:c.787+1542_787+1561dup ENSP00000417148.1:n.787+1542_787+1561dup
ENST00000471181.6:c.2329_2348dup ENSP00000418960.2:p.Ser784MetfsTer15
ENST00000478531.5:c.784+1542_784+1561dup ENSP00000420412.1:n.784+1542_784+1561dup
ENST00000484087.5:c.409+1542_409+1561dup ENSP00000419481.1:n.409+1542_409+1561dup
ENST00000487825.5:c.412+1542_412+1561dup ENSP00000418212.1:n.412+1542_412+1561dup
ENST00000491747.6:c.787+1542_787+1561dup ENSP00000420705.2:n.787+1542_787+1561dup
ENST00000493795.5:c.2188_2207dup ENSP00000418775.1:p.Ser737MetfsTer15
ENST00000493919.5:c.646+1542_646+1561dup ENSP00000418819.1:n.646+1542_646+1561dup
ENST00000586385.5:c.5-29251_5-29232dup ENSP00000465818.1:n.5-29251_5-29232dup
ENST00000591534.5:c.-43-18681_-43-18662dup ENSP00000467329.1:n.-43-18681_-43-18662dup
ENST00000591849.5:c.-99+32069_-99+32088dup ENSP00000465347.1:n.-99+32069_-99+32088dup
ENST00000634433.1:c.2206_2225dup ENSP00000489431.1:p.Ser743MetfsTer15
NM_007294.3:c.2329_2348dup , LRG_292t1:c.2329_2348dup NP_009225.1:p.Ser784MetfsTer15
NM_007297.3:c.2188_2207dup NP_009228.2:p.Ser737MetfsTer15
NM_007298.3:c.787+1542_787+1561dup NP_009229.2:n.787+1542_787+1561dup
NM_007299.3:c.787+1542_787+1561dup NP_009230.2:n.787+1542_787+1561dup
NM_007300.3:c.2329_2348dup NP_009231.2:p.Ser784MetfsTer15
NR_027676.1:n.2465_2484dup
NM_007294.4:c.2329_2348dup MANE Select NP_009225.1:p.Ser784MetfsTer15
NM_007297.4:c.2188_2207dup NP_009228.2:p.Ser737MetfsTer15
NM_007299.4:c.787+1542_787+1561dup NP_009230.2:n.787+1542_787+1561dup
NM_007300.4:c.2329_2348dup NP_009231.2:p.Ser784MetfsTer15
NR_027676.2:n.2506_2525dup