Canonical Allele Identifier: CA2260783729

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43093228_43093229delinsCT , CM000679.2:g.43093228_43093229delinsCT	GRCh38
NC_000017.10:g.41245245_41245246delinsCT , CM000679.1:g.41245245_41245246delinsCT	GRCh37
NC_000017.9:g.38498771_38498772delinsCT	NCBI36
NG_005905.2:g.124755_124756delinsAG , LRG_292:g.124755_124756delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.2366_2367delinsAG
ENST00000461574.2:c.2302_2303delinsAG	ENSP00000417241.2:p.Ser768=
ENST00000470026.6:c.2302_2303delinsAG	ENSP00000419274.2:p.Ser768=
ENST00000473961.6:c.2176_2177delinsAG	ENSP00000420201.2:p.Ser726=
ENST00000476777.6:c.2299_2300delinsAG	ENSP00000417554.2:p.Ser767=
ENST00000477152.6:c.2224_2225delinsAG	ENSP00000419988.2:p.Ser742=
ENST00000478531.6:c.784+1515_784+1516delinsAG	ENSP00000420412.2:n.784+1515_784+1516delinsAG
ENST00000489037.2:c.2224_2225delinsAG	ENSP00000420781.2:p.Ser742=
ENST00000493919.6:c.646+1515_646+1516delinsAG	ENSP00000418819.2:n.646+1515_646+1516delinsAG
ENST00000494123.6:c.2302_2303delinsAG	ENSP00000419103.2:p.Ser768=
ENST00000497488.2:c.1414_1415delinsAG	ENSP00000418986.2:p.Ser472=
ENST00000618469.2:c.2302_2303delinsAG	ENSP00000478114.2:p.Ser768=
ENST00000634433.2:c.2179_2180delinsAG	ENSP00000489431.2:p.Ser727=
ENST00000644379.2:c.2302_2303delinsAG	ENSP00000496570.2:p.Ser768=
ENST00000644555.2:c.646+1515_646+1516delinsAG	ENSP00000494614.2:n.646+1515_646+1516delinsAG
ENST00000652672.2:c.2161_2162delinsAG	ENSP00000498906.2:p.Ser721=
ENST00000484087.6:c.664+1515_664+1516delinsAG	ENSP00000419481.2:n.664+1515_664+1516delinsAG
ENST00000700182.1:c.706+1515_706+1516delinsAG	ENSP00000514849.1:n.706+1515_706+1516delinsAG
ENST00000357654.9:c.2302_2303delinsAG MANE Select	ENSP00000350283.3:p.Ser768=
ENST00000471181.7:c.2302_2303delinsAG	ENSP00000418960.2:p.Ser768=
ENST00000352993.7:c.671-2197_671-2196delinsAG	ENSP00000312236.5:n.671-2197_671-2196delinsAG
ENST00000354071.7:c.2302_2303delinsAG	ENSP00000326002.7:p.Ser768=
ENST00000357654.7:c.2302_2303delinsAG	ENSP00000350283.3:p.Ser768=
ENST00000461221.5:c.*2085_*2086delinsAG	ENSP00000418548.1:n.*2085_*2086delinsAG
ENST00000468300.5:c.787+1515_787+1516delinsAG	ENSP00000417148.1:n.787+1515_787+1516delinsAG
ENST00000471181.6:c.2302_2303delinsAG	ENSP00000418960.2:p.Ser768=
ENST00000478531.5:c.784+1515_784+1516delinsAG	ENSP00000420412.1:n.784+1515_784+1516delinsAG
ENST00000484087.5:c.409+1515_409+1516delinsAG	ENSP00000419481.1:n.409+1515_409+1516delinsAG
ENST00000487825.5:c.412+1515_412+1516delinsAG	ENSP00000418212.1:n.412+1515_412+1516delinsAG
ENST00000491747.6:c.787+1515_787+1516delinsAG	ENSP00000420705.2:n.787+1515_787+1516delinsAG
ENST00000493795.5:c.2161_2162delinsAG	ENSP00000418775.1:p.Ser721=
ENST00000493919.5:c.646+1515_646+1516delinsAG	ENSP00000418819.1:n.646+1515_646+1516delinsAG
ENST00000586385.5:c.5-29278_5-29277delinsAG	ENSP00000465818.1:n.5-29278_5-29277delinsAG
ENST00000591534.5:c.-43-18708_-43-18707delinsAG	ENSP00000467329.1:n.-43-18708_-43-18707delinsAG
ENST00000591849.5:c.-99+32042_-99+32043delinsAG	ENSP00000465347.1:n.-99+32042_-99+32043delinsAG
ENST00000634433.1:c.2179_2180delinsAG	ENSP00000489431.1:p.Ser727=
NM_007294.3:c.2302_2303delinsAG , LRG_292t1:c.2302_2303delinsAG	NP_009225.1:p.Ser768=
NM_007297.3:c.2161_2162delinsAG	NP_009228.2:p.Ser721=
NM_007298.3:c.787+1515_787+1516delinsAG	NP_009229.2:n.787+1515_787+1516delinsAG
NM_007299.3:c.787+1515_787+1516delinsAG	NP_009230.2:n.787+1515_787+1516delinsAG
NM_007300.3:c.2302_2303delinsAG	NP_009231.2:p.Ser768=
NR_027676.1:n.2438_2439delinsAG
NM_007294.4:c.2302_2303delinsAG MANE Select	NP_009225.1:p.Ser768=
NM_007297.4:c.2161_2162delinsAG	NP_009228.2:p.Ser721=
NM_007299.4:c.787+1515_787+1516delinsAG	NP_009230.2:n.787+1515_787+1516delinsAG
NM_007300.4:c.2302_2303delinsAG	NP_009231.2:p.Ser768=
NR_027676.2:n.2479_2480delinsAG