Canonical Allele Identifier: CA2260772475
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43070245T= , CM000679.2:g.43070245T= GRCh38
NC_000017.10:g.41222262T= , CM000679.1:g.41222262T= GRCh37
NC_000017.9:g.38475788T= NCBI36
NG_005905.2:g.147739A= , LRG_292:g.147739A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.4983+683A= ENSP00000417241.2:n.4983+683A=
ENST00000470026.6:c.4986+683A= ENSP00000419274.2:n.4986+683A=
ENST00000473961.6:c.4860+683A= ENSP00000420201.2:n.4860+683A=
ENST00000476777.6:c.4980+683A= ENSP00000417554.2:n.4980+683A=
ENST00000477152.6:c.4908+683A= ENSP00000419988.2:n.4908+683A=
ENST00000478531.6:c.1674+683A= ENSP00000420412.2:n.1674+683A=
ENST00000489037.2:c.4908+683A= ENSP00000420781.2:n.4908+683A=
ENST00000493919.6:c.1536+683A= ENSP00000418819.2:n.1536+683A=
ENST00000494123.6:c.4986+683A= ENSP00000419103.2:n.4986+683A=
ENST00000497488.2:c.4098+683A= ENSP00000418986.2:n.4098+683A=
ENST00000618469.2:c.4986+683A= ENSP00000478114.2:n.4986+683A=
ENST00000634433.2:c.4863+683A= ENSP00000489431.2:n.4863+683A=
ENST00000644379.2:c.5052+683A= ENSP00000496570.2:n.5052+683A=
ENST00000644555.2:c.1536+683A= ENSP00000494614.2:n.1536+683A=
ENST00000652672.2:c.4845+683A= ENSP00000498906.2:n.4845+683A=
ENST00000484087.6:c.1548+683A= ENSP00000419481.2:n.1548+683A=
ENST00000357654.9:c.4986+683A= MANE Select ENSP00000350283.3:n.4986+683A=
ENST00000471181.7:c.5049+683A= ENSP00000418960.2:n.5049+683A=
ENST00000644379.1:c.1373+683A=
ENST00000352993.7:c.1560+683A= ENSP00000312236.5:n.1560+683A=
ENST00000357654.7:c.4986+683A= ENSP00000350283.3:n.4986+683A=
ENST00000461221.5:c.*4769+683A= ENSP00000418548.1:n.*4769+683A=
ENST00000468300.5:c.1674+683A= ENSP00000417148.1:n.1674+683A=
ENST00000471181.6:c.5049+683A= ENSP00000418960.2:n.5049+683A=
ENST00000472490.1:n.139+683A=
ENST00000478531.5:c.1674+683A= ENSP00000420412.1:n.1674+683A=
ENST00000484087.5:c.1299+683A= ENSP00000419481.1:n.1299+683A=
ENST00000491747.6:c.1674+683A= ENSP00000420705.2:n.1674+683A=
ENST00000493795.5:c.4845+683A= ENSP00000418775.1:n.4845+683A=
ENST00000493919.5:c.1536+683A= ENSP00000418819.1:n.1536+683A=
ENST00000586385.5:c.5-6294A= ENSP00000465818.1:n.5-6294A=
ENST00000591534.5:c.459+683A= ENSP00000467329.1:n.459+683A=
ENST00000591849.5:c.-98-20055A= ENSP00000465347.1:n.-98-20055A=
NM_007294.3:c.4986+683A= , LRG_292t1:c.4986+683A= NP_009225.1:n.4986+683A=
NM_007297.3:c.4845+683A= NP_009228.2:n.4845+683A=
NM_007298.3:c.1674+683A= NP_009229.2:n.1674+683A=
NM_007299.3:c.1674+683A= NP_009230.2:n.1674+683A=
NM_007300.3:c.5049+683A= NP_009231.2:n.5049+683A=
NR_027676.1:n.5122+683A=
NM_007294.4:c.4986+683A= MANE Select NP_009225.1:n.4986+683A=
NM_007297.4:c.4845+683A= NP_009228.2:n.4845+683A=
NM_007299.4:c.1674+683A= NP_009230.2:n.1674+683A=
NM_007300.4:c.5049+683A= NP_009231.2:n.5049+683A=
NR_027676.2:n.5163+683A=