Canonical Allele Identifier: CA2638061669
Gene: BRCA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43067146del , CM000679.2:g.43067146del GRCh38
NC_000017.10:g.41219163del , CM000679.1:g.41219163del GRCh37
NC_000017.9:g.38472689del NCBI36
NG_005905.2:g.150841del , LRG_292:g.150841del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5071+465del ENSP00000417241.2:n.5071+465del
ENST00000470026.6:c.5074+465del ENSP00000419274.2:n.5074+465del
ENST00000473961.6:c.4948+465del ENSP00000420201.2:n.4948+465del
ENST00000476777.6:c.5068+465del ENSP00000417554.2:n.5068+465del
ENST00000477152.6:c.4996+465del ENSP00000419988.2:n.4996+465del
ENST00000478531.6:c.1762+465del ENSP00000420412.2:n.1762+465del
ENST00000489037.2:c.4996+465del ENSP00000420781.2:n.4996+465del
ENST00000493919.6:c.1624+465del ENSP00000418819.2:n.1624+465del
ENST00000494123.6:c.5074+465del ENSP00000419103.2:n.5074+465del
ENST00000497488.2:c.4186+465del ENSP00000418986.2:n.4186+465del
ENST00000618469.2:c.5074+465del ENSP00000478114.2:n.5074+465del
ENST00000634433.2:c.4951+465del ENSP00000489431.2:n.4951+465del
ENST00000644379.2:c.5140+465del ENSP00000496570.2:n.5140+465del
ENST00000644555.2:c.1624+465del ENSP00000494614.2:n.1624+465del
ENST00000652672.2:c.4933+465del ENSP00000498906.2:n.4933+465del
ENST00000484087.6:c.1636+465del ENSP00000419481.2:n.1636+465del
ENST00000357654.9:c.5074+465del MANE Select ENSP00000350283.3:n.5074+465del
ENST00000471181.7:c.5137+465del ENSP00000418960.2:n.5137+465del
ENST00000644379.1:c.1461+465del
ENST00000352993.7:c.1648+465del ENSP00000312236.5:n.1648+465del
ENST00000357654.7:c.5074+465del ENSP00000350283.3:n.5074+465del
ENST00000461221.5:c.*4857+465del ENSP00000418548.1:n.*4857+465del
ENST00000468300.5:c.1762+465del ENSP00000417148.1:n.1762+465del
ENST00000471181.6:c.5137+465del ENSP00000418960.2:n.5137+465del
ENST00000478531.5:c.1762+465del ENSP00000420412.1:n.1762+465del
ENST00000484087.5:c.1387+465del ENSP00000419481.1:n.1387+465del
ENST00000491747.6:c.1762+465del ENSP00000420705.2:n.1762+465del
ENST00000493795.5:c.4933+465del ENSP00000418775.1:n.4933+465del
ENST00000493919.5:c.1624+465del ENSP00000418819.1:n.1624+465del
ENST00000586385.5:c.5-3192del ENSP00000465818.1:n.5-3192del
ENST00000591534.5:c.547+465del ENSP00000467329.1:n.547+465del
ENST00000591849.5:c.-98-16953del ENSP00000465347.1:n.-98-16953del
NM_007294.3:c.5074+465del , LRG_292t1:c.5074+465del NP_009225.1:n.5074+465del
NM_007297.3:c.4933+465del NP_009228.2:n.4933+465del
NM_007298.3:c.1762+465del NP_009229.2:n.1762+465del
NM_007299.3:c.1762+465del NP_009230.2:n.1762+465del
NM_007300.3:c.5137+465del NP_009231.2:n.5137+465del
NR_027676.1:n.5210+465del
NM_007294.4:c.5074+465del MANE Select NP_009225.1:n.5074+465del
NM_007297.4:c.4933+465del NP_009228.2:n.4933+465del
NM_007299.4:c.1762+465del NP_009230.2:n.1762+465del
NM_007300.4:c.5137+465del NP_009231.2:n.5137+465del
NR_027676.2:n.5251+465del