Canonical Allele Identifier: CA1139664785

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 928534
• ClinVar RCV Id: RCV003158437
• dbSNP Id: rs2053829800

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43093449_43093453delinsACTGC , CM000679.2:g.43093449_43093453delinsACTGC	GRCh38
NC_000017.10:g.41245466_41245470delinsACTGC , CM000679.1:g.41245466_41245470delinsACTGC	GRCh37
NC_000017.9:g.38498992_38498996delinsACTGC	NCBI36
NG_005905.2:g.124531_124535delinsGCAGT , LRG_292:g.124531_124535delinsGCAGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000354071.8:n.2142_2146delinsGCAGT
ENST00000461574.2:c.2078_2082delinsGCAGT	ENSP00000417241.2:p.Asp693Gly
ENST00000470026.6:c.2078_2082delinsGCAGT	ENSP00000419274.2:p.Asp693Gly
ENST00000473961.6:c.1952_1956delinsGCAGT	ENSP00000420201.2:p.Asp651Gly
ENST00000476777.6:c.2075_2079delinsGCAGT	ENSP00000417554.2:p.Asp692Gly
ENST00000477152.6:c.2000_2004delinsGCAGT	ENSP00000419988.2:p.Asp667Gly
ENST00000478531.6:c.784+1291_784+1295delinsGCAGT	ENSP00000420412.2:n.784+1291_784+1295delinsGCAGT
ENST00000489037.2:c.2000_2004delinsGCAGT	ENSP00000420781.2:p.Asp667Gly
ENST00000493919.6:c.646+1291_646+1295delinsGCAGT	ENSP00000418819.2:n.646+1291_646+1295delinsGCAGT
ENST00000494123.6:c.2078_2082delinsGCAGT	ENSP00000419103.2:p.Asp693Gly
ENST00000497488.2:c.1190_1194delinsGCAGT	ENSP00000418986.2:p.Asp397Gly
ENST00000618469.2:c.2078_2082delinsGCAGT	ENSP00000478114.2:p.Asp693Gly
ENST00000634433.2:c.1955_1959delinsGCAGT	ENSP00000489431.2:p.Asp652Gly
ENST00000644379.2:c.2078_2082delinsGCAGT	ENSP00000496570.2:p.Asp693Gly
ENST00000644555.2:c.646+1291_646+1295delinsGCAGT	ENSP00000494614.2:n.646+1291_646+1295delinsGCAGT
ENST00000652672.2:c.1937_1941delinsGCAGT	ENSP00000498906.2:p.Asp646Gly
ENST00000484087.6:c.664+1291_664+1295delinsGCAGT	ENSP00000419481.2:n.664+1291_664+1295delinsGCAGT
ENST00000700182.1:c.706+1291_706+1295delinsGCAGT	ENSP00000514849.1:n.706+1291_706+1295delinsGCAGT
ENST00000357654.9:c.2078_2082delinsGCAGT MANE Select	ENSP00000350283.3:p.Asp693Gly
ENST00000471181.7:c.2078_2082delinsGCAGT	ENSP00000418960.2:p.Asp693Gly
ENST00000352993.7:c.670+2393_670+2397delinsGCAGT	ENSP00000312236.5:n.670+2393_670+2397delinsGCAGT
ENST00000354071.7:c.2078_2082delinsGCAGT	ENSP00000326002.7:p.Asp693Gly
ENST00000357654.7:c.2078_2082delinsGCAGT	ENSP00000350283.3:p.Asp693Gly
ENST00000461221.5:c.*1861_*1865delinsGCAGT	ENSP00000418548.1:n.*1861_*1865delinsGCAGT
ENST00000468300.5:c.787+1291_787+1295delinsGCAGT	ENSP00000417148.1:n.787+1291_787+1295delinsGCAGT
ENST00000471181.6:c.2078_2082delinsGCAGT	ENSP00000418960.2:p.Asp693Gly
ENST00000478531.5:c.784+1291_784+1295delinsGCAGT	ENSP00000420412.1:n.784+1291_784+1295delinsGCAGT
ENST00000484087.5:c.409+1291_409+1295delinsGCAGT	ENSP00000419481.1:n.409+1291_409+1295delinsGCAGT
ENST00000487825.5:c.412+1291_412+1295delinsGCAGT	ENSP00000418212.1:n.412+1291_412+1295delinsGCAGT
ENST00000491747.6:c.787+1291_787+1295delinsGCAGT	ENSP00000420705.2:n.787+1291_787+1295delinsGCAGT
ENST00000493795.5:c.1937_1941delinsGCAGT	ENSP00000418775.1:p.Asp646Gly
ENST00000493919.5:c.646+1291_646+1295delinsGCAGT	ENSP00000418819.1:n.646+1291_646+1295delinsGCAGT
ENST00000586385.5:c.5-29502_5-29498delinsGCAGT	ENSP00000465818.1:n.5-29502_5-29498delinsGCAGT
ENST00000591534.5:c.-43-18932_-43-18928delinsGCAGT	ENSP00000467329.1:n.-43-18932_-43-18928delinsGCAGT
ENST00000591849.5:c.-99+31818_-99+31822delinsGCAGT	ENSP00000465347.1:n.-99+31818_-99+31822delinsGCAGT
ENST00000634433.1:c.1955_1959delinsGCAGT	ENSP00000489431.1:p.Asp652Gly
NM_007294.3:c.2078_2082delinsGCAGT , LRG_292t1:c.2078_2082delinsGCAGT	NP_009225.1:p.Asp693Gly
NM_007297.3:c.1937_1941delinsGCAGT	NP_009228.2:p.Asp646Gly
NM_007298.3:c.787+1291_787+1295delinsGCAGT	NP_009229.2:n.787+1291_787+1295delinsGCAGT
NM_007299.3:c.787+1291_787+1295delinsGCAGT	NP_009230.2:n.787+1291_787+1295delinsGCAGT
NM_007300.3:c.2078_2082delinsGCAGT	NP_009231.2:p.Asp693Gly
NR_027676.1:n.2214_2218delinsGCAGT
NM_007294.4:c.2078_2082delinsGCAGT MANE Select	NP_009225.1:p.Asp693Gly
NM_007297.4:c.1937_1941delinsGCAGT	NP_009228.2:p.Asp646Gly
NM_007299.4:c.787+1291_787+1295delinsGCAGT	NP_009230.2:n.787+1291_787+1295delinsGCAGT
NM_007300.4:c.2078_2082delinsGCAGT	NP_009231.2:p.Asp693Gly
NR_027676.2:n.2255_2259delinsGCAGT