Canonical Allele Identifier: CA2260784595
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43094082_43094085delinsTATA , CM000679.2:g.43094082_43094085delinsTATA GRCh38
NC_000017.10:g.41246099_41246102delinsTATA , CM000679.1:g.41246099_41246102delinsTATA GRCh37
NC_000017.9:g.38499625_38499628delinsTATA NCBI36
NG_005905.2:g.123899_123902delinsTATA , LRG_292:g.123899_123902delinsTATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.1510_1513delinsTATA
ENST00000461574.2:c.1446_1449delinsTATA ENSP00000417241.2:p.Ile482=
ENST00000470026.6:c.1446_1449delinsTATA ENSP00000419274.2:p.Ile482=
ENST00000473961.6:c.1320_1323delinsTATA ENSP00000420201.2:p.Ile440=
ENST00000476777.6:c.1443_1446delinsTATA ENSP00000417554.2:p.Ile481=
ENST00000477152.6:c.1368_1371delinsTATA ENSP00000419988.2:p.Ile456=
ENST00000478531.6:c.784+659_784+662delinsTATA ENSP00000420412.2:n.784+659_784+662delinsTATA
ENST00000489037.2:c.1368_1371delinsTATA ENSP00000420781.2:p.Ile456=
ENST00000493919.6:c.646+659_646+662delinsTATA ENSP00000418819.2:n.646+659_646+662delinsTATA
ENST00000494123.6:c.1446_1449delinsTATA ENSP00000419103.2:p.Ile482=
ENST00000497488.2:c.558_561delinsTATA ENSP00000418986.2:p.Ile186=
ENST00000618469.2:c.1446_1449delinsTATA ENSP00000478114.2:p.Ile482=
ENST00000634433.2:c.1323_1326delinsTATA ENSP00000489431.2:p.Ile441=
ENST00000644379.2:c.1446_1449delinsTATA ENSP00000496570.2:p.Ile482=
ENST00000644555.2:c.646+659_646+662delinsTATA ENSP00000494614.2:n.646+659_646+662delinsTATA
ENST00000652672.2:c.1305_1308delinsTATA ENSP00000498906.2:p.Ile435=
ENST00000484087.6:c.664+659_664+662delinsTATA ENSP00000419481.2:n.664+659_664+662delinsTATA
ENST00000700182.1:c.706+659_706+662delinsTATA ENSP00000514849.1:n.706+659_706+662delinsTATA
ENST00000700183.1:c.*1454_*1457delinsTATA ENSP00000514850.1:n.*1454_*1457delinsTATA
ENST00000357654.9:c.1446_1449delinsTATA MANE Select ENSP00000350283.3:p.Ile482=
ENST00000471181.7:c.1446_1449delinsTATA ENSP00000418960.2:p.Ile482=
ENST00000652672.1:c.1305_1308delinsTATA ENSP00000498906.1:p.Ile435=
ENST00000352993.7:c.670+1761_670+1764delinsTATA ENSP00000312236.5:n.670+1761_670+1764delinsTATA
ENST00000354071.7:c.1446_1449delinsTATA ENSP00000326002.7:p.Ile482=
ENST00000357654.7:c.1446_1449delinsTATA ENSP00000350283.3:p.Ile482=
ENST00000412061.3:c.797_800delinsTATA
ENST00000461221.5:c.*1229_*1232delinsTATA ENSP00000418548.1:n.*1229_*1232delinsTATA
ENST00000468300.5:c.787+659_787+662delinsTATA ENSP00000417148.1:n.787+659_787+662delinsTATA
ENST00000470026.5:c.1446_1449delinsTATA ENSP00000419274.1:p.Ile482=
ENST00000471181.6:c.1446_1449delinsTATA ENSP00000418960.2:p.Ile482=
ENST00000477152.5:c.1368_1371delinsTATA ENSP00000419988.1:p.Ile456=
ENST00000478531.5:c.784+659_784+662delinsTATA ENSP00000420412.1:n.784+659_784+662delinsTATA
ENST00000484087.5:c.409+659_409+662delinsTATA ENSP00000419481.1:n.409+659_409+662delinsTATA
ENST00000487825.5:c.412+659_412+662delinsTATA ENSP00000418212.1:n.412+659_412+662delinsTATA
ENST00000491747.6:c.787+659_787+662delinsTATA ENSP00000420705.2:n.787+659_787+662delinsTATA
ENST00000493795.5:c.1305_1308delinsTATA ENSP00000418775.1:p.Ile435=
ENST00000493919.5:c.646+659_646+662delinsTATA ENSP00000418819.1:n.646+659_646+662delinsTATA
ENST00000586385.5:c.5-30134_5-30131delinsTATA ENSP00000465818.1:n.5-30134_5-30131delinsTATA
ENST00000591534.5:c.-43-19564_-43-19561delinsTATA ENSP00000467329.1:n.-43-19564_-43-19561delinsTATA
ENST00000591849.5:c.-99+31186_-99+31189delinsTATA ENSP00000465347.1:n.-99+31186_-99+31189delinsTATA
ENST00000634433.1:c.1323_1326delinsTATA ENSP00000489431.1:p.Ile441=
NM_007294.3:c.1446_1449delinsTATA , LRG_292t1:c.1446_1449delinsTATA NP_009225.1:p.Ile482=
NM_007297.3:c.1305_1308delinsTATA NP_009228.2:p.Ile435=
NM_007298.3:c.787+659_787+662delinsTATA NP_009229.2:n.787+659_787+662delinsTATA
NM_007299.3:c.787+659_787+662delinsTATA NP_009230.2:n.787+659_787+662delinsTATA
NM_007300.3:c.1446_1449delinsTATA NP_009231.2:p.Ile482=
NR_027676.1:n.1582_1585delinsTATA
NM_007294.4:c.1446_1449delinsTATA MANE Select NP_009225.1:p.Ile482=
NM_007297.4:c.1305_1308delinsTATA NP_009228.2:p.Ile435=
NM_007299.4:c.787+659_787+662delinsTATA NP_009230.2:n.787+659_787+662delinsTATA
NM_007300.4:c.1446_1449delinsTATA NP_009231.2:p.Ile482=
NR_027676.2:n.1623_1626delinsTATA