Canonical Allele Identifier: CA2260771131
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43067296_43067308delinsCCAGGCTGGAATG , CM000679.2:g.43067296_43067308delinsCCAGGCTGGAATG GRCh38
NC_000017.10:g.41219313_41219325delinsCCAGGCTGGAATG , CM000679.1:g.41219313_41219325delinsCCAGGCTGGAATG GRCh37
NC_000017.9:g.38472839_38472851delinsCCAGGCTGGAATG NCBI36
NG_005905.2:g.150676_150688delinsCATTCCAGCCTGG , LRG_292:g.150676_150688delinsCATTCCAGCCTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5071+300_5071+312delinsCATTCCAGCCTGG ENSP00000417241.2:n.5071+300_5071+312delinsCATTCCAGCCTGG
ENST00000470026.6:c.5074+300_5074+312delinsCATTCCAGCCTGG ENSP00000419274.2:n.5074+300_5074+312delinsCATTCCAGCCTGG
ENST00000473961.6:c.4948+300_4948+312delinsCATTCCAGCCTGG ENSP00000420201.2:n.4948+300_4948+312delinsCATTCCAGCCTGG
ENST00000476777.6:c.5068+300_5068+312delinsCATTCCAGCCTGG ENSP00000417554.2:n.5068+300_5068+312delinsCATTCCAGCCTGG
ENST00000477152.6:c.4996+300_4996+312delinsCATTCCAGCCTGG ENSP00000419988.2:n.4996+300_4996+312delinsCATTCCAGCCTGG
ENST00000478531.6:c.1762+300_1762+312delinsCATTCCAGCCTGG ENSP00000420412.2:n.1762+300_1762+312delinsCATTCCAGCCTGG
ENST00000489037.2:c.4996+300_4996+312delinsCATTCCAGCCTGG ENSP00000420781.2:n.4996+300_4996+312delinsCATTCCAGCCTGG
ENST00000493919.6:c.1624+300_1624+312delinsCATTCCAGCCTGG ENSP00000418819.2:n.1624+300_1624+312delinsCATTCCAGCCTGG
ENST00000494123.6:c.5074+300_5074+312delinsCATTCCAGCCTGG ENSP00000419103.2:n.5074+300_5074+312delinsCATTCCAGCCTGG
ENST00000497488.2:c.4186+300_4186+312delinsCATTCCAGCCTGG ENSP00000418986.2:n.4186+300_4186+312delinsCATTCCAGCCTGG
ENST00000618469.2:c.5074+300_5074+312delinsCATTCCAGCCTGG ENSP00000478114.2:n.5074+300_5074+312delinsCATTCCAGCCTGG
ENST00000634433.2:c.4951+300_4951+312delinsCATTCCAGCCTGG ENSP00000489431.2:n.4951+300_4951+312delinsCATTCCAGCCTGG
ENST00000644379.2:c.5140+300_5140+312delinsCATTCCAGCCTGG ENSP00000496570.2:n.5140+300_5140+312delinsCATTCCAGCCTGG
ENST00000644555.2:c.1624+300_1624+312delinsCATTCCAGCCTGG ENSP00000494614.2:n.1624+300_1624+312delinsCATTCCAGCCTGG
ENST00000652672.2:c.4933+300_4933+312delinsCATTCCAGCCTGG ENSP00000498906.2:n.4933+300_4933+312delinsCATTCCAGCCTGG
ENST00000484087.6:c.1636+300_1636+312delinsCATTCCAGCCTGG ENSP00000419481.2:n.1636+300_1636+312delinsCATTCCAGCCTGG
ENST00000357654.9:c.5074+300_5074+312delinsCATTCCAGCCTGG MANE Select ENSP00000350283.3:n.5074+300_5074+312delinsCATTCCAGCCTGG
ENST00000471181.7:c.5137+300_5137+312delinsCATTCCAGCCTGG ENSP00000418960.2:n.5137+300_5137+312delinsCATTCCAGCCTGG
ENST00000644379.1:c.1461+300_1461+312delinsCATTCCAGCCTGG
ENST00000352993.7:c.1648+300_1648+312delinsCATTCCAGCCTGG ENSP00000312236.5:n.1648+300_1648+312delinsCATTCCAGCCTGG
ENST00000357654.7:c.5074+300_5074+312delinsCATTCCAGCCTGG ENSP00000350283.3:n.5074+300_5074+312delinsCATTCCAGCCTGG
ENST00000461221.5:c.*4857+300_*4857+312delinsCATTCCAGCCTGG ENSP00000418548.1:n.*4857+300_*4857+312delinsCATTCCAGCCTGG
ENST00000468300.5:c.1762+300_1762+312delinsCATTCCAGCCTGG ENSP00000417148.1:n.1762+300_1762+312delinsCATTCCAGCCTGG
ENST00000471181.6:c.5137+300_5137+312delinsCATTCCAGCCTGG ENSP00000418960.2:n.5137+300_5137+312delinsCATTCCAGCCTGG
ENST00000472490.1:n.527_539delinsCATTCCAGCCTGG
ENST00000478531.5:c.1762+300_1762+312delinsCATTCCAGCCTGG ENSP00000420412.1:n.1762+300_1762+312delinsCATTCCAGCCTGG
ENST00000484087.5:c.1387+300_1387+312delinsCATTCCAGCCTGG ENSP00000419481.1:n.1387+300_1387+312delinsCATTCCAGCCTGG
ENST00000491747.6:c.1762+300_1762+312delinsCATTCCAGCCTGG ENSP00000420705.2:n.1762+300_1762+312delinsCATTCCAGCCTGG
ENST00000493795.5:c.4933+300_4933+312delinsCATTCCAGCCTGG ENSP00000418775.1:n.4933+300_4933+312delinsCATTCCAGCCTGG
ENST00000493919.5:c.1624+300_1624+312delinsCATTCCAGCCTGG ENSP00000418819.1:n.1624+300_1624+312delinsCATTCCAGCCTGG
ENST00000586385.5:c.5-3357_5-3345delinsCATTCCAGCCTGG ENSP00000465818.1:n.5-3357_5-3345delinsCATTCCAGCCTGG
ENST00000591534.5:c.547+300_547+312delinsCATTCCAGCCTGG ENSP00000467329.1:n.547+300_547+312delinsCATTCCAGCCTGG
ENST00000591849.5:c.-98-17118_-98-17106delinsCATTCCAGCCTGG ENSP00000465347.1:n.-98-17118_-98-17106delinsCATTCCAGCCTGG
NM_007294.3:c.5074+300_5074+312delinsCATTCCAGCCTGG , LRG_292t1:c.5074+300_5074+312delinsCATTCCAGCCTGG NP_009225.1:n.5074+300_5074+312delinsCATTCCAGCCTGG
NM_007297.3:c.4933+300_4933+312delinsCATTCCAGCCTGG NP_009228.2:n.4933+300_4933+312delinsCATTCCAGCCTGG
NM_007298.3:c.1762+300_1762+312delinsCATTCCAGCCTGG NP_009229.2:n.1762+300_1762+312delinsCATTCCAGCCTGG
NM_007299.3:c.1762+300_1762+312delinsCATTCCAGCCTGG NP_009230.2:n.1762+300_1762+312delinsCATTCCAGCCTGG
NM_007300.3:c.5137+300_5137+312delinsCATTCCAGCCTGG NP_009231.2:n.5137+300_5137+312delinsCATTCCAGCCTGG
NR_027676.1:n.5210+300_5210+312delinsCATTCCAGCCTGG
NM_007294.4:c.5074+300_5074+312delinsCATTCCAGCCTGG MANE Select NP_009225.1:n.5074+300_5074+312delinsCATTCCAGCCTGG
NM_007297.4:c.4933+300_4933+312delinsCATTCCAGCCTGG NP_009228.2:n.4933+300_4933+312delinsCATTCCAGCCTGG
NM_007299.4:c.1762+300_1762+312delinsCATTCCAGCCTGG NP_009230.2:n.1762+300_1762+312delinsCATTCCAGCCTGG
NM_007300.4:c.5137+300_5137+312delinsCATTCCAGCCTGG NP_009231.2:n.5137+300_5137+312delinsCATTCCAGCCTGG
NR_027676.2:n.5251+300_5251+312delinsCATTCCAGCCTGG