Canonical Allele Identifier: CA2825002539

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 3072257
• ClinVar RCV Id: RCV004012287

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43093280_43093282del , CM000679.2:g.43093280_43093282del	GRCh38
NC_000017.10:g.41245297_41245299del , CM000679.1:g.41245297_41245299del	GRCh37
NC_000017.9:g.38498823_38498825del	NCBI36
NG_005905.2:g.124703_124705del , LRG_292:g.124703_124705del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.2314_2316del
ENST00000461574.2:c.2250_2252del	ENSP00000417241.2:p.Met751del
ENST00000470026.6:c.2250_2252del	ENSP00000419274.2:p.Met751del
ENST00000473961.6:c.2124_2126del	ENSP00000420201.2:p.Met709del
ENST00000476777.6:c.2247_2249del	ENSP00000417554.2:p.Met750del
ENST00000477152.6:c.2172_2174del	ENSP00000419988.2:p.Met725del
ENST00000478531.6:c.784+1463_784+1465del	ENSP00000420412.2:n.784+1463_784+1465del
ENST00000489037.2:c.2172_2174del	ENSP00000420781.2:p.Met725del
ENST00000493919.6:c.646+1463_646+1465del	ENSP00000418819.2:n.646+1463_646+1465del
ENST00000494123.6:c.2250_2252del	ENSP00000419103.2:p.Met751del
ENST00000497488.2:c.1362_1364del	ENSP00000418986.2:p.Met455del
ENST00000618469.2:c.2250_2252del	ENSP00000478114.2:p.Met751del
ENST00000634433.2:c.2127_2129del	ENSP00000489431.2:p.Met710del
ENST00000644379.2:c.2250_2252del	ENSP00000496570.2:p.Met751del
ENST00000644555.2:c.646+1463_646+1465del	ENSP00000494614.2:n.646+1463_646+1465del
ENST00000652672.2:c.2109_2111del	ENSP00000498906.2:p.Met704del
ENST00000484087.6:c.664+1463_664+1465del	ENSP00000419481.2:n.664+1463_664+1465del
ENST00000700182.1:c.706+1463_706+1465del	ENSP00000514849.1:n.706+1463_706+1465del
ENST00000357654.9:c.2250_2252del MANE Select	ENSP00000350283.3:p.Met751del
ENST00000471181.7:c.2250_2252del	ENSP00000418960.2:p.Met751del
ENST00000352993.7:c.671-2249_671-2247del	ENSP00000312236.5:n.671-2249_671-2247del
ENST00000354071.7:c.2250_2252del	ENSP00000326002.7:p.Met751del
ENST00000357654.7:c.2250_2252del	ENSP00000350283.3:p.Met751del
ENST00000461221.5:c.*2033_*2035del	ENSP00000418548.1:n.*2033_*2035del
ENST00000468300.5:c.787+1463_787+1465del	ENSP00000417148.1:n.787+1463_787+1465del
ENST00000471181.6:c.2250_2252del	ENSP00000418960.2:p.Met751del
ENST00000478531.5:c.784+1463_784+1465del	ENSP00000420412.1:n.784+1463_784+1465del
ENST00000484087.5:c.409+1463_409+1465del	ENSP00000419481.1:n.409+1463_409+1465del
ENST00000487825.5:c.412+1463_412+1465del	ENSP00000418212.1:n.412+1463_412+1465del
ENST00000491747.6:c.787+1463_787+1465del	ENSP00000420705.2:n.787+1463_787+1465del
ENST00000493795.5:c.2109_2111del	ENSP00000418775.1:p.Met704del
ENST00000493919.5:c.646+1463_646+1465del	ENSP00000418819.1:n.646+1463_646+1465del
ENST00000586385.5:c.5-29330_5-29328del	ENSP00000465818.1:n.5-29330_5-29328del
ENST00000591534.5:c.-43-18760_-43-18758del	ENSP00000467329.1:n.-43-18760_-43-18758del
ENST00000591849.5:c.-99+31990_-99+31992del	ENSP00000465347.1:n.-99+31990_-99+31992del
ENST00000634433.1:c.2127_2129del	ENSP00000489431.1:p.Met710del
NM_007294.3:c.2250_2252del , LRG_292t1:c.2250_2252del	NP_009225.1:p.Met751del
NM_007297.3:c.2109_2111del	NP_009228.2:p.Met704del
NM_007298.3:c.787+1463_787+1465del	NP_009229.2:n.787+1463_787+1465del
NM_007299.3:c.787+1463_787+1465del	NP_009230.2:n.787+1463_787+1465del
NM_007300.3:c.2250_2252del	NP_009231.2:p.Met751del
NR_027676.1:n.2386_2388del
NM_007294.4:c.2250_2252del MANE Select	NP_009225.1:p.Met751del
NM_007297.4:c.2109_2111del	NP_009228.2:p.Met704del
NM_007299.4:c.787+1463_787+1465del	NP_009230.2:n.787+1463_787+1465del
NM_007300.4:c.2250_2252del	NP_009231.2:p.Met751del
NR_027676.2:n.2427_2429del