Canonical Allele Identifier: CA10600637
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43094807T>C , CM000679.2:g.43094807T>C GRCh38
NC_000017.10:g.41246824T>C , CM000679.1:g.41246824T>C GRCh37
NC_000017.9:g.38500350T>C NCBI36
NG_005905.2:g.123177A>G , LRG_292:g.123177A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.788A>G
ENST00000461574.2:c.724A>G ENSP00000417241.2:p.Ser242Gly
ENST00000470026.6:c.724A>G ENSP00000419274.2:p.Ser242Gly
ENST00000473961.6:c.598A>G ENSP00000420201.2:p.Ser200Gly
ENST00000476777.6:c.721A>G ENSP00000417554.2:p.Ser241Gly
ENST00000477152.6:c.646A>G ENSP00000419988.2:p.Ser216Gly
ENST00000478531.6:c.721A>G ENSP00000420412.2:p.Ser241Gly
ENST00000489037.2:c.646A>G ENSP00000420781.2:p.Ser216Gly
ENST00000493919.6:c.583A>G ENSP00000418819.2:p.Ser195Gly
ENST00000494123.6:c.724A>G ENSP00000419103.2:p.Ser242Gly
ENST00000497488.2:c.-165A>G ENSP00000418986.2:n.-165A>G
ENST00000618469.2:c.724A>G ENSP00000478114.2:p.Ser242Gly
ENST00000634433.2:c.601A>G ENSP00000489431.2:p.Ser201Gly
ENST00000644379.2:c.724A>G ENSP00000496570.2:p.Ser242Gly
ENST00000644555.2:c.583A>G ENSP00000494614.2:p.Ser195Gly
ENST00000652672.2:c.583A>G ENSP00000498906.2:p.Ser195Gly
ENST00000484087.6:c.601A>G ENSP00000419481.2:p.Ser201Gly
ENST00000700182.1:c.643A>G ENSP00000514849.1:p.Ser215Gly
ENST00000700183.1:c.*732A>G ENSP00000514850.1:n.*732A>G
ENST00000357654.9:c.724A>G MANE Select ENSP00000350283.3:p.Ser242Gly
ENST00000471181.7:c.724A>G ENSP00000418960.2:p.Ser242Gly
ENST00000642945.1:c.*598A>G ENSP00000495897.1:n.*598A>G
ENST00000652672.1:c.583A>G ENSP00000498906.1:p.Ser195Gly
ENST00000352993.7:c.670+1039A>G ENSP00000312236.5:n.670+1039A>G
ENST00000354071.7:c.724A>G ENSP00000326002.7:p.Ser242Gly
ENST00000357654.7:c.724A>G ENSP00000350283.3:p.Ser242Gly
ENST00000412061.3:c.75A>G
ENST00000461221.5:c.*507A>G ENSP00000418548.1:n.*507A>G
ENST00000468300.5:c.724A>G ENSP00000417148.1:p.Ser242Gly
ENST00000470026.5:c.724A>G ENSP00000419274.1:p.Ser242Gly
ENST00000471181.6:c.724A>G ENSP00000418960.2:p.Ser242Gly
ENST00000473961.5:c.321A>G
ENST00000477152.5:c.646A>G ENSP00000419988.1:p.Ser216Gly
ENST00000478531.5:c.721A>G ENSP00000420412.1:p.Ser241Gly
ENST00000484087.5:c.346A>G ENSP00000419481.1:p.Ser116Gly
ENST00000487825.5:c.349A>G ENSP00000418212.1:p.Ser117Gly
ENST00000491747.6:c.724A>G ENSP00000420705.2:p.Ser242Gly
ENST00000492859.5:c.*660A>G ENSP00000420253.1:n.*660A>G
ENST00000493795.5:c.583A>G ENSP00000418775.1:p.Ser195Gly
ENST00000493919.5:c.583A>G ENSP00000418819.1:p.Ser195Gly
ENST00000494123.5:c.724A>G ENSP00000419103.1:p.Ser242Gly
ENST00000497488.1:c.-165A>G ENSP00000418986.1:n.-165A>G
ENST00000586385.5:c.4+30375A>G ENSP00000465818.1:n.4+30375A>G
ENST00000591534.5:c.-43-20286A>G ENSP00000467329.1:n.-43-20286A>G
ENST00000591849.5:c.-99+30464A>G ENSP00000465347.1:n.-99+30464A>G
ENST00000634433.1:c.601A>G ENSP00000489431.1:p.Ser201Gly
NM_007294.3:c.724A>G , LRG_292t1:c.724A>G NP_009225.1:p.Ser242Gly
NM_007297.3:c.583A>G NP_009228.2:p.Ser195Gly
NM_007298.3:c.724A>G NP_009229.2:p.Ser242Gly
NM_007299.3:c.724A>G NP_009230.2:p.Ser242Gly
NM_007300.3:c.724A>G NP_009231.2:p.Ser242Gly
NR_027676.1:n.860A>G
NM_007294.4:c.724A>G MANE Select NP_009225.1:p.Ser242Gly
NM_007297.4:c.583A>G NP_009228.2:p.Ser195Gly
NM_007299.4:c.724A>G NP_009230.2:p.Ser242Gly
NM_007300.4:c.724A>G NP_009231.2:p.Ser242Gly
NR_027676.2:n.901A>G