Canonical Allele Identifier: CA2260766303
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43056943G= , CM000679.2:g.43056943G= GRCh38
NC_000017.10:g.41208960G= , CM000679.1:g.41208960G= GRCh37
NC_000017.9:g.38462486G= NCBI36
NG_005905.2:g.161041C= , LRG_292:g.161041C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5274+109C= ENSP00000417241.2:n.5274+109C=
ENST00000470026.6:c.5277+109C= ENSP00000419274.2:n.5277+109C=
ENST00000473961.6:c.5151+109C= ENSP00000420201.2:n.5151+109C=
ENST00000476777.6:c.5271+109C= ENSP00000417554.2:n.5271+109C=
ENST00000477152.6:c.5199+109C= ENSP00000419988.2:n.5199+109C=
ENST00000478531.6:c.1965+109C= ENSP00000420412.2:n.1965+109C=
ENST00000489037.2:c.5199+109C= ENSP00000420781.2:n.5199+109C=
ENST00000493919.6:c.1827+109C= ENSP00000418819.2:n.1827+109C=
ENST00000494123.6:c.5277+109C= ENSP00000419103.2:n.5277+109C=
ENST00000497488.2:c.4389+109C= ENSP00000418986.2:n.4389+109C=
ENST00000618469.2:c.5277+109C= ENSP00000478114.2:n.5277+109C=
ENST00000634433.2:c.5154+109C= ENSP00000489431.2:n.5154+109C=
ENST00000644379.2:c.5343+109C= ENSP00000496570.2:n.5343+109C=
ENST00000644555.2:c.1827+109C= ENSP00000494614.2:n.1827+109C=
ENST00000652672.2:c.5136+109C= ENSP00000498906.2:n.5136+109C=
ENST00000484087.6:c.1839+109C= ENSP00000419481.2:n.1839+109C=
ENST00000357654.9:c.5277+109C= MANE Select ENSP00000350283.3:n.5277+109C=
ENST00000471181.7:c.5340+109C= ENSP00000418960.2:n.5340+109C=
ENST00000644379.1:c.1664+109C=
ENST00000352993.7:c.1851+109C= ENSP00000312236.5:n.1851+109C=
ENST00000357654.7:c.5277+109C= ENSP00000350283.3:n.5277+109C=
ENST00000461221.5:c.*5060+109C= ENSP00000418548.1:n.*5060+109C=
ENST00000468300.5:c.1965+109C= ENSP00000417148.1:n.1965+109C=
ENST00000471181.6:c.5340+109C= ENSP00000418960.2:n.5340+109C=
ENST00000491747.6:c.1965+109C= ENSP00000420705.2:n.1965+109C=
ENST00000493795.5:c.5136+109C= ENSP00000418775.1:n.5136+109C=
ENST00000586385.5:c.207+109C= ENSP00000465818.1:n.207+109C=
ENST00000591534.5:c.750+109C= ENSP00000467329.1:n.750+109C=
ENST00000591849.5:c.-98-6753C= ENSP00000465347.1:n.-98-6753C=
NM_007294.3:c.5277+109C= , LRG_292t1:c.5277+109C= NP_009225.1:n.5277+109C=
NM_007297.3:c.5136+109C= NP_009228.2:n.5136+109C=
NM_007298.3:c.1965+109C= NP_009229.2:n.1965+109C=
NM_007299.3:c.1965+109C= NP_009230.2:n.1965+109C=
NM_007300.3:c.5340+109C= NP_009231.2:n.5340+109C=
NR_027676.1:n.5413+109C=
NM_007294.4:c.5277+109C= MANE Select NP_009225.1:n.5277+109C=
NM_007297.4:c.5136+109C= NP_009228.2:n.5136+109C=
NM_007299.4:c.1965+109C= NP_009230.2:n.1965+109C=
NM_007300.4:c.5340+109C= NP_009231.2:n.5340+109C=
NR_027676.2:n.5454+109C=