Canonical Allele Identifier: CA915950128

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 663277
• ClinVar RCV Id: RCV000821128 ; RCV001283887
• dbSNP Id: rs1597874930

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43093889_43093890insC , CM000679.2:g.43093889_43093890insC	GRCh38
NC_000017.10:g.41245906_41245907insC , CM000679.1:g.41245906_41245907insC	GRCh37
NC_000017.9:g.38499432_38499433insC	NCBI36
NG_005905.2:g.124094_124095insG , LRG_292:g.124094_124095insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000354071.8:n.1705_1706insG
ENST00000461574.2:c.1641_1642insG	ENSP00000417241.2:p.Ile548AspfsTer3
ENST00000470026.6:c.1641_1642insG	ENSP00000419274.2:p.Ile548AspfsTer3
ENST00000473961.6:c.1515_1516insG	ENSP00000420201.2:p.Ile506AspfsTer3
ENST00000476777.6:c.1638_1639insG	ENSP00000417554.2:p.Ile547AspfsTer3
ENST00000477152.6:c.1563_1564insG	ENSP00000419988.2:p.Ile522AspfsTer3
ENST00000478531.6:c.784+854_784+855insG	ENSP00000420412.2:n.784+854_784+855insG
ENST00000489037.2:c.1563_1564insG	ENSP00000420781.2:p.Ile522AspfsTer3
ENST00000493919.6:c.646+854_646+855insG	ENSP00000418819.2:n.646+854_646+855insG
ENST00000494123.6:c.1641_1642insG	ENSP00000419103.2:p.Ile548AspfsTer3
ENST00000497488.2:c.753_754insG	ENSP00000418986.2:p.Ile252AspfsTer3
ENST00000618469.2:c.1641_1642insG	ENSP00000478114.2:p.Ile548AspfsTer3
ENST00000634433.2:c.1518_1519insG	ENSP00000489431.2:p.Ile507AspfsTer3
ENST00000644379.2:c.1641_1642insG	ENSP00000496570.2:p.Ile548AspfsTer3
ENST00000644555.2:c.646+854_646+855insG	ENSP00000494614.2:n.646+854_646+855insG
ENST00000652672.2:c.1500_1501insG	ENSP00000498906.2:p.Ile501AspfsTer3
ENST00000484087.6:c.664+854_664+855insG	ENSP00000419481.2:n.664+854_664+855insG
ENST00000700182.1:c.706+854_706+855insG	ENSP00000514849.1:n.706+854_706+855insG
ENST00000357654.9:c.1641_1642insG MANE Select	ENSP00000350283.3:p.Ile548AspfsTer3
ENST00000471181.7:c.1641_1642insG	ENSP00000418960.2:p.Ile548AspfsTer3
ENST00000652672.1:c.1500_1501insG	ENSP00000498906.1:p.Ile501AspfsTer3
ENST00000352993.7:c.670+1956_670+1957insG	ENSP00000312236.5:n.670+1956_670+1957insG...
ENST00000354071.7:c.1641_1642insG	ENSP00000326002.7:p.Ile548AspfsTer3
ENST00000357654.7:c.1641_1642insG	ENSP00000350283.3:p.Ile548AspfsTer3
ENST00000412061.3:c.992_993insG
ENST00000461221.5:c.*1424_*1425insG	ENSP00000418548.1:n.*1424_*1425insG
ENST00000468300.5:c.787+854_787+855insG	ENSP00000417148.1:n.787+854_787+855insG
ENST00000470026.5:c.1641_1642insG	ENSP00000419274.1:p.Ile548AspfsTer3
ENST00000471181.6:c.1641_1642insG	ENSP00000418960.2:p.Ile548AspfsTer3
ENST00000477152.5:c.1563_1564insG	ENSP00000419988.1:p.Ile522AspfsTer3
ENST00000478531.5:c.784+854_784+855insG	ENSP00000420412.1:n.784+854_784+855insG
ENST00000484087.5:c.409+854_409+855insG	ENSP00000419481.1:n.409+854_409+855insG
ENST00000487825.5:c.412+854_412+855insG	ENSP00000418212.1:n.412+854_412+855insG
ENST00000491747.6:c.787+854_787+855insG	ENSP00000420705.2:n.787+854_787+855insG
ENST00000493795.5:c.1500_1501insG	ENSP00000418775.1:p.Ile501AspfsTer3
ENST00000493919.5:c.646+854_646+855insG	ENSP00000418819.1:n.646+854_646+855insG
ENST00000586385.5:c.5-29939_5-29938insG	ENSP00000465818.1:n.5-29939_5-29938insG
ENST00000591534.5:c.-43-19369_-43-19368insG	ENSP00000467329.1:n.-43-19369_-43-19368in...
ENST00000591849.5:c.-99+31381_-99+31382insG	ENSP00000465347.1:n.-99+31381_-99+31382in...
ENST00000634433.1:c.1518_1519insG	ENSP00000489431.1:p.Ile507AspfsTer3
NM_007294.3:c.1641_1642insG , LRG_292t1:c.1641_1642insG	NP_009225.1:p.Ile548AspfsTer3
NM_007297.3:c.1500_1501insG	NP_009228.2:p.Ile501AspfsTer3
NM_007298.3:c.787+854_787+855insG	NP_009229.2:n.787+854_787+855insG
NM_007299.3:c.787+854_787+855insG	NP_009230.2:n.787+854_787+855insG
NM_007300.3:c.1641_1642insG	NP_009231.2:p.Ile548AspfsTer3
NR_027676.1:n.1777_1778insG
NM_007294.4:c.1641_1642insG MANE Select	NP_009225.1:p.Ile548AspfsTer3
NM_007297.4:c.1500_1501insG	NP_009228.2:p.Ile501AspfsTer3
NM_007299.4:c.787+854_787+855insG	NP_009230.2:n.787+854_787+855insG
NM_007300.4:c.1641_1642insG	NP_009231.2:p.Ile548AspfsTer3
NR_027676.2:n.1818_1819insG