Canonical Allele Identifier: CA2809539232
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43067277_43067282del , CM000679.2:g.43067277_43067282del GRCh38
NC_000017.10:g.41219294_41219299del , CM000679.1:g.41219294_41219299del GRCh37
NC_000017.9:g.38472820_38472825del NCBI36
NG_005905.2:g.150705_150710del , LRG_292:g.150705_150710del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5071+329_5071+334del ENSP00000417241.2:n.5071+329_5071+334del
ENST00000470026.6:c.5074+329_5074+334del ENSP00000419274.2:n.5074+329_5074+334del
ENST00000473961.6:c.4948+329_4948+334del ENSP00000420201.2:n.4948+329_4948+334del
ENST00000476777.6:c.5068+329_5068+334del ENSP00000417554.2:n.5068+329_5068+334del
ENST00000477152.6:c.4996+329_4996+334del ENSP00000419988.2:n.4996+329_4996+334del
ENST00000478531.6:c.1762+329_1762+334del ENSP00000420412.2:n.1762+329_1762+334del
ENST00000489037.2:c.4996+329_4996+334del ENSP00000420781.2:n.4996+329_4996+334del
ENST00000493919.6:c.1624+329_1624+334del ENSP00000418819.2:n.1624+329_1624+334del
ENST00000494123.6:c.5074+329_5074+334del ENSP00000419103.2:n.5074+329_5074+334del
ENST00000497488.2:c.4186+329_4186+334del ENSP00000418986.2:n.4186+329_4186+334del
ENST00000618469.2:c.5074+329_5074+334del ENSP00000478114.2:n.5074+329_5074+334del
ENST00000634433.2:c.4951+329_4951+334del ENSP00000489431.2:n.4951+329_4951+334del
ENST00000644379.2:c.5140+329_5140+334del ENSP00000496570.2:n.5140+329_5140+334del
ENST00000644555.2:c.1624+329_1624+334del ENSP00000494614.2:n.1624+329_1624+334del
ENST00000652672.2:c.4933+329_4933+334del ENSP00000498906.2:n.4933+329_4933+334del
ENST00000484087.6:c.1636+329_1636+334del ENSP00000419481.2:n.1636+329_1636+334del
ENST00000357654.9:c.5074+329_5074+334del MANE Select ENSP00000350283.3:n.5074+329_5074+334del
ENST00000471181.7:c.5137+329_5137+334del ENSP00000418960.2:n.5137+329_5137+334del
ENST00000644379.1:c.1461+329_1461+334del
ENST00000352993.7:c.1648+329_1648+334del ENSP00000312236.5:n.1648+329_1648+334del
ENST00000357654.7:c.5074+329_5074+334del ENSP00000350283.3:n.5074+329_5074+334del
ENST00000461221.5:c.*4857+329_*4857+334del ENSP00000418548.1:n.*4857+329_*4857+334del
ENST00000468300.5:c.1762+329_1762+334del ENSP00000417148.1:n.1762+329_1762+334del
ENST00000471181.6:c.5137+329_5137+334del ENSP00000418960.2:n.5137+329_5137+334del
ENST00000472490.1:n.556_561del
ENST00000478531.5:c.1762+329_1762+334del ENSP00000420412.1:n.1762+329_1762+334del
ENST00000484087.5:c.1387+329_1387+334del ENSP00000419481.1:n.1387+329_1387+334del
ENST00000491747.6:c.1762+329_1762+334del ENSP00000420705.2:n.1762+329_1762+334del
ENST00000493795.5:c.4933+329_4933+334del ENSP00000418775.1:n.4933+329_4933+334del
ENST00000493919.5:c.1624+329_1624+334del ENSP00000418819.1:n.1624+329_1624+334del
ENST00000586385.5:c.5-3328_5-3323del ENSP00000465818.1:n.5-3328_5-3323del
ENST00000591534.5:c.547+329_547+334del ENSP00000467329.1:n.547+329_547+334del
ENST00000591849.5:c.-98-17089_-98-17084del ENSP00000465347.1:n.-98-17089_-98-17084del
NM_007294.3:c.5074+329_5074+334del , LRG_292t1:c.5074+329_5074+334del NP_009225.1:n.5074+329_5074+334del
NM_007297.3:c.4933+329_4933+334del NP_009228.2:n.4933+329_4933+334del
NM_007298.3:c.1762+329_1762+334del NP_009229.2:n.1762+329_1762+334del
NM_007299.3:c.1762+329_1762+334del NP_009230.2:n.1762+329_1762+334del
NM_007300.3:c.5137+329_5137+334del NP_009231.2:n.5137+329_5137+334del
NR_027676.1:n.5210+329_5210+334del
NM_007294.4:c.5074+329_5074+334del MANE Select NP_009225.1:n.5074+329_5074+334del
NM_007297.4:c.4933+329_4933+334del NP_009228.2:n.4933+329_4933+334del
NM_007299.4:c.1762+329_1762+334del NP_009230.2:n.1762+329_1762+334del
NM_007300.4:c.5137+329_5137+334del NP_009231.2:n.5137+329_5137+334del
NR_027676.2:n.5251+329_5251+334del