Canonical Allele Identifier: CA2580094095

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 2030561
• ClinVar RCV Id: RCV002848425

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43093468_43093469del , CM000679.2:g.43093468_43093469del	GRCh38
NC_000017.10:g.41245485_41245486del , CM000679.1:g.41245485_41245486del	GRCh37
NC_000017.9:g.38499011_38499012del	NCBI36
NG_005905.2:g.124516_124517del , LRG_292:g.124516_124517del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.2127_2128del
ENST00000461574.2:c.2063_2064del	ENSP00000417241.2:p.Thr688LysfsTer2
ENST00000470026.6:c.2063_2064del	ENSP00000419274.2:p.Thr688LysfsTer2
ENST00000473961.6:c.1937_1938del	ENSP00000420201.2:p.Thr646LysfsTer2
ENST00000476777.6:c.2060_2061del	ENSP00000417554.2:p.Thr687LysfsTer2
ENST00000477152.6:c.1985_1986del	ENSP00000419988.2:p.Thr662LysfsTer2
ENST00000478531.6:c.784+1276_784+1277del	ENSP00000420412.2:n.784+1276_784+1277del
ENST00000489037.2:c.1985_1986del	ENSP00000420781.2:p.Thr662LysfsTer2
ENST00000493919.6:c.646+1276_646+1277del	ENSP00000418819.2:n.646+1276_646+1277del
ENST00000494123.6:c.2063_2064del	ENSP00000419103.2:p.Thr688LysfsTer2
ENST00000497488.2:c.1175_1176del	ENSP00000418986.2:p.Thr392LysfsTer2
ENST00000618469.2:c.2063_2064del	ENSP00000478114.2:p.Thr688LysfsTer2
ENST00000634433.2:c.1940_1941del	ENSP00000489431.2:p.Thr647LysfsTer2
ENST00000644379.2:c.2063_2064del	ENSP00000496570.2:p.Thr688LysfsTer2
ENST00000644555.2:c.646+1276_646+1277del	ENSP00000494614.2:n.646+1276_646+1277del
ENST00000652672.2:c.1922_1923del	ENSP00000498906.2:p.Thr641LysfsTer2
ENST00000484087.6:c.664+1276_664+1277del	ENSP00000419481.2:n.664+1276_664+1277del
ENST00000700182.1:c.706+1276_706+1277del	ENSP00000514849.1:n.706+1276_706+1277del
ENST00000357654.9:c.2063_2064del MANE Select	ENSP00000350283.3:p.Thr688LysfsTer2
ENST00000471181.7:c.2063_2064del	ENSP00000418960.2:p.Thr688LysfsTer2
ENST00000352993.7:c.670+2378_670+2379del	ENSP00000312236.5:n.670+2378_670+2379del
ENST00000354071.7:c.2063_2064del	ENSP00000326002.7:p.Thr688LysfsTer2
ENST00000357654.7:c.2063_2064del	ENSP00000350283.3:p.Thr688LysfsTer2
ENST00000461221.5:c.*1846_*1847del	ENSP00000418548.1:n.*1846_*1847del
ENST00000468300.5:c.787+1276_787+1277del	ENSP00000417148.1:n.787+1276_787+1277del
ENST00000471181.6:c.2063_2064del	ENSP00000418960.2:p.Thr688LysfsTer2
ENST00000478531.5:c.784+1276_784+1277del	ENSP00000420412.1:n.784+1276_784+1277del
ENST00000484087.5:c.409+1276_409+1277del	ENSP00000419481.1:n.409+1276_409+1277del
ENST00000487825.5:c.412+1276_412+1277del	ENSP00000418212.1:n.412+1276_412+1277del
ENST00000491747.6:c.787+1276_787+1277del	ENSP00000420705.2:n.787+1276_787+1277del
ENST00000493795.5:c.1922_1923del	ENSP00000418775.1:p.Thr641LysfsTer2
ENST00000493919.5:c.646+1276_646+1277del	ENSP00000418819.1:n.646+1276_646+1277del
ENST00000586385.5:c.5-29517_5-29516del	ENSP00000465818.1:n.5-29517_5-29516del
ENST00000591534.5:c.-43-18947_-43-18946del	ENSP00000467329.1:n.-43-18947_-43-18946del
ENST00000591849.5:c.-99+31803_-99+31804del	ENSP00000465347.1:n.-99+31803_-99+31804del
ENST00000634433.1:c.1940_1941del	ENSP00000489431.1:p.Thr647LysfsTer2
NM_007294.3:c.2063_2064del , LRG_292t1:c.2063_2064del	NP_009225.1:p.Thr688LysfsTer2
NM_007297.3:c.1922_1923del	NP_009228.2:p.Thr641LysfsTer2
NM_007298.3:c.787+1276_787+1277del	NP_009229.2:n.787+1276_787+1277del
NM_007299.3:c.787+1276_787+1277del	NP_009230.2:n.787+1276_787+1277del
NM_007300.3:c.2063_2064del	NP_009231.2:p.Thr688LysfsTer2
NR_027676.1:n.2199_2200del
NM_007294.4:c.2063_2064del MANE Select	NP_009225.1:p.Thr688LysfsTer2
NM_007297.4:c.1922_1923del	NP_009228.2:p.Thr641LysfsTer2
NM_007299.4:c.787+1276_787+1277del	NP_009230.2:n.787+1276_787+1277del
NM_007300.4:c.2063_2064del	NP_009231.2:p.Thr688LysfsTer2
NR_027676.2:n.2240_2241del