Canonical Allele Identifier: CA001388

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 125539
• ClinVar RCV Id: RCV000111769
• dbSNP Id: rs483353086
• MyVariant Identifiers: chr17:g.41245449_41245450insT (hg19) ; chr17:g.43093432_43093433insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43093432_43093433insT , CM000679.2:g.43093432_43093433insT	GRCh38
NC_000017.10:g.41245449_41245450insT , CM000679.1:g.41245449_41245450insT	GRCh37
NC_000017.9:g.38498975_38498976insT	NCBI36
NG_005905.2:g.124551_124552insA , LRG_292:g.124551_124552insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.2162_2163insA
ENST00000461574.2:c.2098_2099insA	ENSP00000417241.2:p.Leu700HisfsTer12
ENST00000470026.6:c.2098_2099insA	ENSP00000419274.2:p.Leu700HisfsTer12
ENST00000473961.6:c.1972_1973insA	ENSP00000420201.2:p.Leu658HisfsTer12
ENST00000476777.6:c.2095_2096insA	ENSP00000417554.2:p.Leu699HisfsTer12
ENST00000477152.6:c.2020_2021insA	ENSP00000419988.2:p.Leu674HisfsTer12
ENST00000478531.6:c.784+1311_784+1312insA	ENSP00000420412.2:n.784+1311_784+1312insA
ENST00000489037.2:c.2020_2021insA	ENSP00000420781.2:p.Leu674HisfsTer12
ENST00000493919.6:c.646+1311_646+1312insA	ENSP00000418819.2:n.646+1311_646+1312insA
ENST00000494123.6:c.2098_2099insA	ENSP00000419103.2:p.Leu700HisfsTer12
ENST00000497488.2:c.1210_1211insA	ENSP00000418986.2:p.Leu404HisfsTer12
ENST00000618469.2:c.2098_2099insA	ENSP00000478114.2:p.Leu700HisfsTer12
ENST00000634433.2:c.1975_1976insA	ENSP00000489431.2:p.Leu659HisfsTer12
ENST00000644379.2:c.2098_2099insA	ENSP00000496570.2:p.Leu700HisfsTer12
ENST00000644555.2:c.646+1311_646+1312insA	ENSP00000494614.2:n.646+1311_646+1312insA
ENST00000652672.2:c.1957_1958insA	ENSP00000498906.2:p.Leu653HisfsTer12
ENST00000484087.6:c.664+1311_664+1312insA	ENSP00000419481.2:n.664+1311_664+1312insA
ENST00000700182.1:c.706+1311_706+1312insA	ENSP00000514849.1:n.706+1311_706+1312insA
ENST00000357654.9:c.2098_2099insA MANE Select	ENSP00000350283.3:p.Leu700HisfsTer12
ENST00000471181.7:c.2098_2099insA	ENSP00000418960.2:p.Leu700HisfsTer12
ENST00000352993.7:c.671-2401_671-2400insA	ENSP00000312236.5:n.671-2401_671-2400insA
ENST00000354071.7:c.2098_2099insA	ENSP00000326002.7:p.Leu700HisfsTer12
ENST00000357654.7:c.2098_2099insA	ENSP00000350283.3:p.Leu700HisfsTer12
ENST00000461221.5:c.*1881_*1882insA	ENSP00000418548.1:n.*1881_*1882insA
ENST00000468300.5:c.787+1311_787+1312insA	ENSP00000417148.1:n.787+1311_787+1312insA
ENST00000471181.6:c.2098_2099insA	ENSP00000418960.2:p.Leu700HisfsTer12
ENST00000478531.5:c.784+1311_784+1312insA	ENSP00000420412.1:n.784+1311_784+1312insA
ENST00000484087.5:c.409+1311_409+1312insA	ENSP00000419481.1:n.409+1311_409+1312insA
ENST00000487825.5:c.412+1311_412+1312insA	ENSP00000418212.1:n.412+1311_412+1312insA
ENST00000491747.6:c.787+1311_787+1312insA	ENSP00000420705.2:n.787+1311_787+1312insA
ENST00000493795.5:c.1957_1958insA	ENSP00000418775.1:p.Leu653HisfsTer12
ENST00000493919.5:c.646+1311_646+1312insA	ENSP00000418819.1:n.646+1311_646+1312insA
ENST00000586385.5:c.5-29482_5-29481insA	ENSP00000465818.1:n.5-29482_5-29481insA
ENST00000591534.5:c.-43-18912_-43-18911insA	ENSP00000467329.1:n.-43-18912_-43-18911insA
ENST00000591849.5:c.-99+31838_-99+31839insA	ENSP00000465347.1:n.-99+31838_-99+31839insA
ENST00000634433.1:c.1975_1976insA	ENSP00000489431.1:p.Leu659HisfsTer12
NM_007294.3:c.2098_2099insA , LRG_292t1:c.2098_2099insA	NP_009225.1:p.Leu700HisfsTer12
NM_007297.3:c.1957_1958insA	NP_009228.2:p.Leu653HisfsTer12
NM_007298.3:c.787+1311_787+1312insA	NP_009229.2:n.787+1311_787+1312insA
NM_007299.3:c.787+1311_787+1312insA	NP_009230.2:n.787+1311_787+1312insA
NM_007300.3:c.2098_2099insA	NP_009231.2:p.Leu700HisfsTer12
NR_027676.1:n.2234_2235insA
NM_007294.4:c.2098_2099insA MANE Select	NP_009225.1:p.Leu700HisfsTer12
NM_007297.4:c.1957_1958insA	NP_009228.2:p.Leu653HisfsTer12
NM_007299.4:c.787+1311_787+1312insA	NP_009230.2:n.787+1311_787+1312insA
NM_007300.4:c.2098_2099insA	NP_009231.2:p.Leu700HisfsTer12
NR_027676.2:n.2275_2276insA