Canonical Allele Identifier: CA10599664
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 954592
dbSNP Id: rs2053980032

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43094339A>C , CM000679.2:g.43094339A>C GRCh38
NC_000017.10:g.41246356A>C , CM000679.1:g.41246356A>C GRCh37
NC_000017.9:g.38499882A>C NCBI36
NG_005905.2:g.123645T>G , LRG_292:g.123645T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.1256T>G
ENST00000461574.2:c.1192T>G ENSP00000417241.2:p.Ser398Ala
ENST00000470026.6:c.1192T>G ENSP00000419274.2:p.Ser398Ala
ENST00000473961.6:c.1066T>G ENSP00000420201.2:p.Ser356Ala
ENST00000476777.6:c.1189T>G ENSP00000417554.2:p.Ser397Ala
ENST00000477152.6:c.1114T>G ENSP00000419988.2:p.Ser372Ala
ENST00000478531.6:c.784+405T>G ENSP00000420412.2:n.784+405T>G
ENST00000489037.2:c.1114T>G ENSP00000420781.2:p.Ser372Ala
ENST00000493919.6:c.646+405T>G ENSP00000418819.2:n.646+405T>G
ENST00000494123.6:c.1192T>G ENSP00000419103.2:p.Ser398Ala
ENST00000497488.2:c.304T>G ENSP00000418986.2:p.Ser102Ala
ENST00000618469.2:c.1192T>G ENSP00000478114.2:p.Ser398Ala
ENST00000634433.2:c.1069T>G ENSP00000489431.2:p.Ser357Ala
ENST00000644379.2:c.1192T>G ENSP00000496570.2:p.Ser398Ala
ENST00000644555.2:c.646+405T>G ENSP00000494614.2:n.646+405T>G
ENST00000652672.2:c.1051T>G ENSP00000498906.2:p.Ser351Ala
ENST00000484087.6:c.664+405T>G ENSP00000419481.2:n.664+405T>G
ENST00000700182.1:c.706+405T>G ENSP00000514849.1:n.706+405T>G
ENST00000700183.1:c.*1200T>G ENSP00000514850.1:n.*1200T>G
ENST00000357654.9:c.1192T>G MANE Select ENSP00000350283.3:p.Ser398Ala
ENST00000471181.7:c.1192T>G ENSP00000418960.2:p.Ser398Ala
ENST00000652672.1:c.1051T>G ENSP00000498906.1:p.Ser351Ala
ENST00000352993.7:c.670+1507T>G ENSP00000312236.5:n.670+1507T>G
ENST00000354071.7:c.1192T>G ENSP00000326002.7:p.Ser398Ala
ENST00000357654.7:c.1192T>G ENSP00000350283.3:p.Ser398Ala
ENST00000412061.3:c.543T>G
ENST00000461221.5:c.*975T>G ENSP00000418548.1:n.*975T>G
ENST00000468300.5:c.787+405T>G ENSP00000417148.1:n.787+405T>G
ENST00000470026.5:c.1192T>G ENSP00000419274.1:p.Ser398Ala
ENST00000471181.6:c.1192T>G ENSP00000418960.2:p.Ser398Ala
ENST00000473961.5:c.789T>G
ENST00000477152.5:c.1114T>G ENSP00000419988.1:p.Ser372Ala
ENST00000478531.5:c.784+405T>G ENSP00000420412.1:n.784+405T>G
ENST00000484087.5:c.409+405T>G ENSP00000419481.1:n.409+405T>G
ENST00000487825.5:c.412+405T>G ENSP00000418212.1:n.412+405T>G
ENST00000491747.6:c.787+405T>G ENSP00000420705.2:n.787+405T>G
ENST00000492859.5:c.*1128T>G ENSP00000420253.1:n.*1128T>G
ENST00000493795.5:c.1051T>G ENSP00000418775.1:p.Ser351Ala
ENST00000493919.5:c.646+405T>G ENSP00000418819.1:n.646+405T>G
ENST00000494123.5:c.1192T>G ENSP00000419103.1:p.Ser398Ala
ENST00000497488.1:c.304T>G ENSP00000418986.1:p.Ser102Ala
ENST00000586385.5:c.5-30388T>G ENSP00000465818.1:n.5-30388T>G
ENST00000591534.5:c.-43-19818T>G ENSP00000467329.1:n.-43-19818T>G
ENST00000591849.5:c.-99+30932T>G ENSP00000465347.1:n.-99+30932T>G
ENST00000634433.1:c.1069T>G ENSP00000489431.1:p.Ser357Ala
NM_007294.3:c.1192T>G , LRG_292t1:c.1192T>G NP_009225.1:p.Ser398Ala
NM_007297.3:c.1051T>G NP_009228.2:p.Ser351Ala
NM_007298.3:c.787+405T>G NP_009229.2:n.787+405T>G
NM_007299.3:c.787+405T>G NP_009230.2:n.787+405T>G
NM_007300.3:c.1192T>G NP_009231.2:p.Ser398Ala
NR_027676.1:n.1328T>G
NM_007294.4:c.1192T>G MANE Select NP_009225.1:p.Ser398Ala
NM_007297.4:c.1051T>G NP_009228.2:p.Ser351Ala
NM_007299.4:c.787+405T>G NP_009230.2:n.787+405T>G
NM_007300.4:c.1192T>G NP_009231.2:p.Ser398Ala
NR_027676.2:n.1369T>G