Canonical Allele Identifier: CA2260783846

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43093332_43093335delinsCTCT , CM000679.2:g.43093332_43093335delinsCTCT	GRCh38
NC_000017.10:g.41245349_41245352delinsCTCT , CM000679.1:g.41245349_41245352delinsCTCT	GRCh37
NC_000017.9:g.38498875_38498878delinsCTCT	NCBI36
NG_005905.2:g.124649_124652delinsAGAG , LRG_292:g.124649_124652delinsAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.2260_2263delinsAGAG
ENST00000461574.2:c.2196_2199delinsAGAG	ENSP00000417241.2:p.Glu732=
ENST00000470026.6:c.2196_2199delinsAGAG	ENSP00000419274.2:p.Glu732=
ENST00000473961.6:c.2070_2073delinsAGAG	ENSP00000420201.2:p.Glu690=
ENST00000476777.6:c.2193_2196delinsAGAG	ENSP00000417554.2:p.Glu731=
ENST00000477152.6:c.2118_2121delinsAGAG	ENSP00000419988.2:p.Glu706=
ENST00000478531.6:c.784+1409_784+1412delinsAGAG	ENSP00000420412.2:n.784+1409_784+1412delinsAGAG
ENST00000489037.2:c.2118_2121delinsAGAG	ENSP00000420781.2:p.Glu706=
ENST00000493919.6:c.646+1409_646+1412delinsAGAG	ENSP00000418819.2:n.646+1409_646+1412delinsAGAG
ENST00000494123.6:c.2196_2199delinsAGAG	ENSP00000419103.2:p.Glu732=
ENST00000497488.2:c.1308_1311delinsAGAG	ENSP00000418986.2:p.Glu436=
ENST00000618469.2:c.2196_2199delinsAGAG	ENSP00000478114.2:p.Glu732=
ENST00000634433.2:c.2073_2076delinsAGAG	ENSP00000489431.2:p.Glu691=
ENST00000644379.2:c.2196_2199delinsAGAG	ENSP00000496570.2:p.Glu732=
ENST00000644555.2:c.646+1409_646+1412delinsAGAG	ENSP00000494614.2:n.646+1409_646+1412delinsAGAG
ENST00000652672.2:c.2055_2058delinsAGAG	ENSP00000498906.2:p.Glu685=
ENST00000484087.6:c.664+1409_664+1412delinsAGAG	ENSP00000419481.2:n.664+1409_664+1412delinsAGAG
ENST00000700182.1:c.706+1409_706+1412delinsAGAG	ENSP00000514849.1:n.706+1409_706+1412delinsAGAG
ENST00000357654.9:c.2196_2199delinsAGAG MANE Select	ENSP00000350283.3:p.Glu732=
ENST00000471181.7:c.2196_2199delinsAGAG	ENSP00000418960.2:p.Glu732=
ENST00000352993.7:c.671-2303_671-2300delinsAGAG	ENSP00000312236.5:n.671-2303_671-2300delinsAGAG
ENST00000354071.7:c.2196_2199delinsAGAG	ENSP00000326002.7:p.Glu732=
ENST00000357654.7:c.2196_2199delinsAGAG	ENSP00000350283.3:p.Glu732=
ENST00000461221.5:c.*1979_*1982delinsAGAG	ENSP00000418548.1:n.*1979_*1982delinsAGAG
ENST00000468300.5:c.787+1409_787+1412delinsAGAG	ENSP00000417148.1:n.787+1409_787+1412delinsAGAG
ENST00000471181.6:c.2196_2199delinsAGAG	ENSP00000418960.2:p.Glu732=
ENST00000478531.5:c.784+1409_784+1412delinsAGAG	ENSP00000420412.1:n.784+1409_784+1412delinsAGAG
ENST00000484087.5:c.409+1409_409+1412delinsAGAG	ENSP00000419481.1:n.409+1409_409+1412delinsAGAG
ENST00000487825.5:c.412+1409_412+1412delinsAGAG	ENSP00000418212.1:n.412+1409_412+1412delinsAGAG
ENST00000491747.6:c.787+1409_787+1412delinsAGAG	ENSP00000420705.2:n.787+1409_787+1412delinsAGAG
ENST00000493795.5:c.2055_2058delinsAGAG	ENSP00000418775.1:p.Glu685=
ENST00000493919.5:c.646+1409_646+1412delinsAGAG	ENSP00000418819.1:n.646+1409_646+1412delinsAGAG
ENST00000586385.5:c.5-29384_5-29381delinsAGAG	ENSP00000465818.1:n.5-29384_5-29381delinsAGAG
ENST00000591534.5:c.-43-18814_-43-18811delinsAGAG	ENSP00000467329.1:n.-43-18814_-43-18811delinsAGAG
ENST00000591849.5:c.-99+31936_-99+31939delinsAGAG	ENSP00000465347.1:n.-99+31936_-99+31939delinsAGAG
ENST00000634433.1:c.2073_2076delinsAGAG	ENSP00000489431.1:p.Glu691=
NM_007294.3:c.2196_2199delinsAGAG , LRG_292t1:c.2196_2199delinsAGAG	NP_009225.1:p.Glu732=
NM_007297.3:c.2055_2058delinsAGAG	NP_009228.2:p.Glu685=
NM_007298.3:c.787+1409_787+1412delinsAGAG	NP_009229.2:n.787+1409_787+1412delinsAGAG
NM_007299.3:c.787+1409_787+1412delinsAGAG	NP_009230.2:n.787+1409_787+1412delinsAGAG
NM_007300.3:c.2196_2199delinsAGAG	NP_009231.2:p.Glu732=
NR_027676.1:n.2332_2335delinsAGAG
NM_007294.4:c.2196_2199delinsAGAG MANE Select	NP_009225.1:p.Glu732=
NM_007297.4:c.2055_2058delinsAGAG	NP_009228.2:p.Glu685=
NM_007299.4:c.787+1409_787+1412delinsAGAG	NP_009230.2:n.787+1409_787+1412delinsAGAG
NM_007300.4:c.2196_2199delinsAGAG	NP_009231.2:p.Glu732=
NR_027676.2:n.2373_2376delinsAGAG