Canonical Allele Identifier: CA2260771351
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43067642A= , CM000679.2:g.43067642A= GRCh38
NC_000017.10:g.41219659A= , CM000679.1:g.41219659A= GRCh37
NC_000017.9:g.38473185A= NCBI36
NG_005905.2:g.150342T= , LRG_292:g.150342T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5037T= ENSP00000417241.2:p.Ile1679=
ENST00000470026.6:c.5040T= ENSP00000419274.2:p.Ile1680=
ENST00000473961.6:c.4914T= ENSP00000420201.2:p.Ile1638=
ENST00000476777.6:c.5034T= ENSP00000417554.2:p.Ile1678=
ENST00000477152.6:c.4962T= ENSP00000419988.2:p.Ile1654=
ENST00000478531.6:c.1728T= ENSP00000420412.2:p.Ile576=
ENST00000489037.2:c.4962T= ENSP00000420781.2:p.Ile1654=
ENST00000493919.6:c.1590T= ENSP00000418819.2:p.Ile530=
ENST00000494123.6:c.5040T= ENSP00000419103.2:p.Ile1680=
ENST00000497488.2:c.4152T= ENSP00000418986.2:p.Ile1384=
ENST00000618469.2:c.5040T= ENSP00000478114.2:p.Ile1680=
ENST00000634433.2:c.4917T= ENSP00000489431.2:p.Ile1639=
ENST00000644379.2:c.5106T= ENSP00000496570.2:p.Ile1702=
ENST00000644555.2:c.1590T= ENSP00000494614.2:p.Ile530=
ENST00000652672.2:c.4899T= ENSP00000498906.2:p.Ile1633=
ENST00000484087.6:c.1602T= ENSP00000419481.2:p.Ile534=
ENST00000357654.9:c.5040T= MANE Select ENSP00000350283.3:p.Ile1680=
ENST00000471181.7:c.5103T= ENSP00000418960.2:p.Ile1701=
ENST00000644379.1:c.1427T=
ENST00000352993.7:c.1614T= ENSP00000312236.5:p.Ile538=
ENST00000357654.7:c.5040T= ENSP00000350283.3:p.Ile1680=
ENST00000461221.5:c.*4823T= ENSP00000418548.1:n.*4823T=
ENST00000468300.5:c.1728T= ENSP00000417148.1:p.Ile576=
ENST00000471181.6:c.5103T= ENSP00000418960.2:p.Ile1701=
ENST00000472490.1:n.193T=
ENST00000478531.5:c.1728T= ENSP00000420412.1:p.Ile576=
ENST00000484087.5:c.1353T= ENSP00000419481.1:p.Ile451=
ENST00000491747.6:c.1728T= ENSP00000420705.2:p.Ile576=
ENST00000493795.5:c.4899T= ENSP00000418775.1:p.Ile1633=
ENST00000493919.5:c.1590T= ENSP00000418819.1:p.Ile530=
ENST00000586385.5:c.5-3691T= ENSP00000465818.1:n.5-3691T=
ENST00000591534.5:c.513T= ENSP00000467329.1:p.Ile171=
ENST00000591849.5:c.-98-17452T= ENSP00000465347.1:n.-98-17452T=
NM_007294.3:c.5040T= , LRG_292t1:c.5040T= NP_009225.1:p.Ile1680=
NM_007297.3:c.4899T= NP_009228.2:p.Ile1633=
NM_007298.3:c.1728T= NP_009229.2:p.Ile576=
NM_007299.3:c.1728T= NP_009230.2:p.Ile576=
NM_007300.3:c.5103T= NP_009231.2:p.Ile1701=
NR_027676.1:n.5176T=
NM_007294.4:c.5040T= MANE Select NP_009225.1:p.Ile1680=
NM_007297.4:c.4899T= NP_009228.2:p.Ile1633=
NM_007299.4:c.1728T= NP_009230.2:p.Ile576=
NM_007300.4:c.5103T= NP_009231.2:p.Ile1701=
NR_027676.2:n.5217T=