Canonical Allele Identifier: CA2260775523
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43076579T= , CM000679.2:g.43076579T= GRCh38
NC_000017.10:g.41228596T= , CM000679.1:g.41228596T= GRCh37
NC_000017.9:g.38482122T= NCBI36
NG_005905.2:g.141405A= , LRG_292:g.141405A=

Transcript Alleles

HGVS Amino-acid change
ENST00000461574.2:c.4390A= ENSP00000417241.2:p.Ile1464=
ENST00000470026.6:c.4393A= ENSP00000419274.2:p.Ile1465=
ENST00000473961.6:c.4267A= ENSP00000420201.2:p.Ile1423=
ENST00000476777.6:c.4387A= ENSP00000417554.2:p.Ile1463=
ENST00000477152.6:c.4315A= ENSP00000419988.2:p.Ile1439=
ENST00000478531.6:c.1081A= ENSP00000420412.2:p.Ile361=
ENST00000489037.2:c.4315A= ENSP00000420781.2:p.Ile1439=
ENST00000493919.6:c.943A= ENSP00000418819.2:p.Ile315=
ENST00000494123.6:c.4393A= ENSP00000419103.2:p.Ile1465=
ENST00000497488.2:c.3505A= ENSP00000418986.2:p.Ile1169=
ENST00000618469.2:c.4393A= ENSP00000478114.2:p.Ile1465=
ENST00000634433.2:c.4270A= ENSP00000489431.2:p.Ile1424=
ENST00000644379.2:c.4459A= ENSP00000496570.2:p.Ile1487=
ENST00000644555.2:c.943A= ENSP00000494614.2:p.Ile315=
ENST00000652672.2:c.4252A= ENSP00000498906.2:p.Ile1418=
ENST00000484087.6:c.955A= ENSP00000419481.2:p.Ile319=
ENST00000700182.1:c.1000A= ENSP00000514849.1:p.Ile334=
ENST00000357654.9:c.4393A= MANE Select ENSP00000350283.3:p.Ile1465=
ENST00000471181.7:c.4456A= ENSP00000418960.2:p.Ile1486=
ENST00000644379.1:c.780A=
ENST00000352993.7:c.967A= ENSP00000312236.5:p.Ile323=
ENST00000357654.7:c.4393A= ENSP00000350283.3:p.Ile1465=
ENST00000461221.5:c.*4176A= ENSP00000418548.1:n.*4176A=
ENST00000461574.1:c.684A=
ENST00000468300.5:c.1081A= ENSP00000417148.1:p.Ile361=
ENST00000471181.6:c.4456A= ENSP00000418960.2:p.Ile1486=
ENST00000478531.5:c.1081A= ENSP00000420412.1:p.Ile361=
ENST00000484087.5:c.706A= ENSP00000419481.1:p.Ile236=
ENST00000487825.5:c.709A= ENSP00000418212.1:p.Ile237=
ENST00000491747.6:c.1081A= ENSP00000420705.2:p.Ile361=
ENST00000493795.5:c.4252A= ENSP00000418775.1:p.Ile1418=
ENST00000493919.5:c.943A= ENSP00000418819.1:p.Ile315=
ENST00000586385.5:c.5-12628A= ENSP00000465818.1:n.5-12628A=
ENST00000591534.5:c.-43-2058A= ENSP00000467329.1:n.-43-2058A=
ENST00000591849.5:c.-98-26389A= ENSP00000465347.1:n.-98-26389A=
ENST00000621897.1:n.284A=
NM_007294.3:c.4393A= , LRG_292t1:c.4393A= NP_009225.1:p.Ile1465=
NM_007297.3:c.4252A= NP_009228.2:p.Ile1418=
NM_007298.3:c.1081A= NP_009229.2:p.Ile361=
NM_007299.3:c.1081A= NP_009230.2:p.Ile361=
NM_007300.3:c.4456A= NP_009231.2:p.Ile1486=
NR_027676.1:n.4529A=
NM_007294.4:c.4393A= MANE Select NP_009225.1:p.Ile1465=
NM_007297.4:c.4252A= NP_009228.2:p.Ile1418=
NM_007299.4:c.1081A= NP_009230.2:p.Ile361=
NM_007300.4:c.4456A= NP_009231.2:p.Ile1486=
NR_027676.2:n.4570A=