Canonical Allele Identifier: CA2260784588
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43094073A= , CM000679.2:g.43094073A= GRCh38
NC_000017.10:g.41246090A= , CM000679.1:g.41246090A= GRCh37
NC_000017.9:g.38499616A= NCBI36
NG_005905.2:g.123911T= , LRG_292:g.123911T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.1522T=
ENST00000461574.2:c.1458T= ENSP00000417241.2:p.Phe486=
ENST00000470026.6:c.1458T= ENSP00000419274.2:p.Phe486=
ENST00000473961.6:c.1332T= ENSP00000420201.2:p.Phe444=
ENST00000476777.6:c.1455T= ENSP00000417554.2:p.Phe485=
ENST00000477152.6:c.1380T= ENSP00000419988.2:p.Phe460=
ENST00000478531.6:c.784+671T= ENSP00000420412.2:n.784+671T=
ENST00000489037.2:c.1380T= ENSP00000420781.2:p.Phe460=
ENST00000493919.6:c.646+671T= ENSP00000418819.2:n.646+671T=
ENST00000494123.6:c.1458T= ENSP00000419103.2:p.Phe486=
ENST00000497488.2:c.570T= ENSP00000418986.2:p.Phe190=
ENST00000618469.2:c.1458T= ENSP00000478114.2:p.Phe486=
ENST00000634433.2:c.1335T= ENSP00000489431.2:p.Phe445=
ENST00000644379.2:c.1458T= ENSP00000496570.2:p.Phe486=
ENST00000644555.2:c.646+671T= ENSP00000494614.2:n.646+671T=
ENST00000652672.2:c.1317T= ENSP00000498906.2:p.Phe439=
ENST00000484087.6:c.664+671T= ENSP00000419481.2:n.664+671T=
ENST00000700182.1:c.706+671T= ENSP00000514849.1:n.706+671T=
ENST00000700183.1:c.*1466T= ENSP00000514850.1:n.*1466T=
ENST00000357654.9:c.1458T= MANE Select ENSP00000350283.3:p.Phe486=
ENST00000471181.7:c.1458T= ENSP00000418960.2:p.Phe486=
ENST00000652672.1:c.1317T= ENSP00000498906.1:p.Phe439=
ENST00000352993.7:c.670+1773T= ENSP00000312236.5:n.670+1773T=
ENST00000354071.7:c.1458T= ENSP00000326002.7:p.Phe486=
ENST00000357654.7:c.1458T= ENSP00000350283.3:p.Phe486=
ENST00000412061.3:c.809T=
ENST00000461221.5:c.*1241T= ENSP00000418548.1:n.*1241T=
ENST00000468300.5:c.787+671T= ENSP00000417148.1:n.787+671T=
ENST00000470026.5:c.1458T= ENSP00000419274.1:p.Phe486=
ENST00000471181.6:c.1458T= ENSP00000418960.2:p.Phe486=
ENST00000477152.5:c.1380T= ENSP00000419988.1:p.Phe460=
ENST00000478531.5:c.784+671T= ENSP00000420412.1:n.784+671T=
ENST00000484087.5:c.409+671T= ENSP00000419481.1:n.409+671T=
ENST00000487825.5:c.412+671T= ENSP00000418212.1:n.412+671T=
ENST00000491747.6:c.787+671T= ENSP00000420705.2:n.787+671T=
ENST00000493795.5:c.1317T= ENSP00000418775.1:p.Phe439=
ENST00000493919.5:c.646+671T= ENSP00000418819.1:n.646+671T=
ENST00000586385.5:c.5-30122T= ENSP00000465818.1:n.5-30122T=
ENST00000591534.5:c.-43-19552T= ENSP00000467329.1:n.-43-19552T=
ENST00000591849.5:c.-99+31198T= ENSP00000465347.1:n.-99+31198T=
ENST00000634433.1:c.1335T= ENSP00000489431.1:p.Phe445=
NM_007294.3:c.1458T= , LRG_292t1:c.1458T= NP_009225.1:p.Phe486=
NM_007297.3:c.1317T= NP_009228.2:p.Phe439=
NM_007298.3:c.787+671T= NP_009229.2:n.787+671T=
NM_007299.3:c.787+671T= NP_009230.2:n.787+671T=
NM_007300.3:c.1458T= NP_009231.2:p.Phe486=
NR_027676.1:n.1594T=
NM_007294.4:c.1458T= MANE Select NP_009225.1:p.Phe486=
NM_007297.4:c.1317T= NP_009228.2:p.Phe439=
NM_007299.4:c.787+671T= NP_009230.2:n.787+671T=
NM_007300.4:c.1458T= NP_009231.2:p.Phe486=
NR_027676.2:n.1635T=