Canonical Allele Identifier: CA2260766318
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43057002T= , CM000679.2:g.43057002T= GRCh38
NC_000017.10:g.41209019T= , CM000679.1:g.41209019T= GRCh37
NC_000017.9:g.38462545T= NCBI36
NG_005905.2:g.160982A= , LRG_292:g.160982A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5274+50A= ENSP00000417241.2:n.5274+50A=
ENST00000470026.6:c.5277+50A= ENSP00000419274.2:n.5277+50A=
ENST00000473961.6:c.5151+50A= ENSP00000420201.2:n.5151+50A=
ENST00000476777.6:c.5271+50A= ENSP00000417554.2:n.5271+50A=
ENST00000477152.6:c.5199+50A= ENSP00000419988.2:n.5199+50A=
ENST00000478531.6:c.1965+50A= ENSP00000420412.2:n.1965+50A=
ENST00000489037.2:c.5199+50A= ENSP00000420781.2:n.5199+50A=
ENST00000493919.6:c.1827+50A= ENSP00000418819.2:n.1827+50A=
ENST00000494123.6:c.5277+50A= ENSP00000419103.2:n.5277+50A=
ENST00000497488.2:c.4389+50A= ENSP00000418986.2:n.4389+50A=
ENST00000618469.2:c.5277+50A= ENSP00000478114.2:n.5277+50A=
ENST00000634433.2:c.5154+50A= ENSP00000489431.2:n.5154+50A=
ENST00000644379.2:c.5343+50A= ENSP00000496570.2:n.5343+50A=
ENST00000644555.2:c.1827+50A= ENSP00000494614.2:n.1827+50A=
ENST00000652672.2:c.5136+50A= ENSP00000498906.2:n.5136+50A=
ENST00000484087.6:c.1839+50A= ENSP00000419481.2:n.1839+50A=
ENST00000357654.9:c.5277+50A= MANE Select ENSP00000350283.3:n.5277+50A=
ENST00000471181.7:c.5340+50A= ENSP00000418960.2:n.5340+50A=
ENST00000644379.1:c.1664+50A=
ENST00000352993.7:c.1851+50A= ENSP00000312236.5:n.1851+50A=
ENST00000357654.7:c.5277+50A= ENSP00000350283.3:n.5277+50A=
ENST00000461221.5:c.*5060+50A= ENSP00000418548.1:n.*5060+50A=
ENST00000468300.5:c.1965+50A= ENSP00000417148.1:n.1965+50A=
ENST00000471181.6:c.5340+50A= ENSP00000418960.2:n.5340+50A=
ENST00000491747.6:c.1965+50A= ENSP00000420705.2:n.1965+50A=
ENST00000493795.5:c.5136+50A= ENSP00000418775.1:n.5136+50A=
ENST00000586385.5:c.207+50A= ENSP00000465818.1:n.207+50A=
ENST00000591534.5:c.750+50A= ENSP00000467329.1:n.750+50A=
ENST00000591849.5:c.-98-6812A= ENSP00000465347.1:n.-98-6812A=
NM_007294.3:c.5277+50A= , LRG_292t1:c.5277+50A= NP_009225.1:n.5277+50A=
NM_007297.3:c.5136+50A= NP_009228.2:n.5136+50A=
NM_007298.3:c.1965+50A= NP_009229.2:n.1965+50A=
NM_007299.3:c.1965+50A= NP_009230.2:n.1965+50A=
NM_007300.3:c.5340+50A= NP_009231.2:n.5340+50A=
NR_027676.1:n.5413+50A=
NM_007294.4:c.5277+50A= MANE Select NP_009225.1:n.5277+50A=
NM_007297.4:c.5136+50A= NP_009228.2:n.5136+50A=
NM_007299.4:c.1965+50A= NP_009230.2:n.1965+50A=
NM_007300.4:c.5340+50A= NP_009231.2:n.5340+50A=
NR_027676.2:n.5454+50A=