Canonical Allele Identifier: CA2260783667
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43093169_43093170delinsCT , CM000679.2:g.43093169_43093170delinsCT GRCh38
NC_000017.10:g.41245186_41245187delinsCT , CM000679.1:g.41245186_41245187delinsCT GRCh37
NC_000017.9:g.38498712_38498713delinsCT NCBI36
NG_005905.2:g.124814_124815delinsAG , LRG_292:g.124814_124815delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.2425_2426delinsAG
ENST00000461574.2:c.2361_2362delinsAG ENSP00000417241.2:p.Glu787=
ENST00000470026.6:c.2361_2362delinsAG ENSP00000419274.2:p.Glu787=
ENST00000473961.6:c.2235_2236delinsAG ENSP00000420201.2:p.Glu745=
ENST00000476777.6:c.2358_2359delinsAG ENSP00000417554.2:p.Glu786=
ENST00000477152.6:c.2283_2284delinsAG ENSP00000419988.2:p.Glu761=
ENST00000478531.6:c.784+1574_784+1575delinsAG ENSP00000420412.2:n.784+1574_784+1575delinsAG
ENST00000489037.2:c.2283_2284delinsAG ENSP00000420781.2:p.Glu761=
ENST00000493919.6:c.646+1574_646+1575delinsAG ENSP00000418819.2:n.646+1574_646+1575delinsAG
ENST00000494123.6:c.2361_2362delinsAG ENSP00000419103.2:p.Glu787=
ENST00000497488.2:c.1473_1474delinsAG ENSP00000418986.2:p.Glu491=
ENST00000618469.2:c.2361_2362delinsAG ENSP00000478114.2:p.Glu787=
ENST00000634433.2:c.2238_2239delinsAG ENSP00000489431.2:p.Glu746=
ENST00000644379.2:c.2361_2362delinsAG ENSP00000496570.2:p.Glu787=
ENST00000644555.2:c.646+1574_646+1575delinsAG ENSP00000494614.2:n.646+1574_646+1575delinsAG
ENST00000652672.2:c.2220_2221delinsAG ENSP00000498906.2:p.Glu740=
ENST00000484087.6:c.664+1574_664+1575delinsAG ENSP00000419481.2:n.664+1574_664+1575delinsAG
ENST00000700182.1:c.706+1574_706+1575delinsAG ENSP00000514849.1:n.706+1574_706+1575delinsAG
ENST00000357654.9:c.2361_2362delinsAG MANE Select ENSP00000350283.3:p.Glu787=
ENST00000471181.7:c.2361_2362delinsAG ENSP00000418960.2:p.Glu787=
ENST00000352993.7:c.671-2138_671-2137delinsAG ENSP00000312236.5:n.671-2138_671-2137delinsAG
ENST00000354071.7:c.2361_2362delinsAG ENSP00000326002.7:p.Glu787=
ENST00000357654.7:c.2361_2362delinsAG ENSP00000350283.3:p.Glu787=
ENST00000461221.5:c.*2144_*2145delinsAG ENSP00000418548.1:n.*2144_*2145delinsAG
ENST00000468300.5:c.787+1574_787+1575delinsAG ENSP00000417148.1:n.787+1574_787+1575delinsAG
ENST00000471181.6:c.2361_2362delinsAG ENSP00000418960.2:p.Glu787=
ENST00000478531.5:c.784+1574_784+1575delinsAG ENSP00000420412.1:n.784+1574_784+1575delinsAG
ENST00000484087.5:c.409+1574_409+1575delinsAG ENSP00000419481.1:n.409+1574_409+1575delinsAG
ENST00000487825.5:c.412+1574_412+1575delinsAG ENSP00000418212.1:n.412+1574_412+1575delinsAG
ENST00000491747.6:c.787+1574_787+1575delinsAG ENSP00000420705.2:n.787+1574_787+1575delinsAG
ENST00000493795.5:c.2220_2221delinsAG ENSP00000418775.1:p.Glu740=
ENST00000493919.5:c.646+1574_646+1575delinsAG ENSP00000418819.1:n.646+1574_646+1575delinsAG
ENST00000586385.5:c.5-29219_5-29218delinsAG ENSP00000465818.1:n.5-29219_5-29218delinsAG
ENST00000591534.5:c.-43-18649_-43-18648delinsAG ENSP00000467329.1:n.-43-18649_-43-18648delinsAG
ENST00000591849.5:c.-99+32101_-99+32102delinsAG ENSP00000465347.1:n.-99+32101_-99+32102delinsAG
ENST00000634433.1:c.2238_2239delinsAG ENSP00000489431.1:p.Glu746=
NM_007294.3:c.2361_2362delinsAG , LRG_292t1:c.2361_2362delinsAG NP_009225.1:p.Glu787=
NM_007297.3:c.2220_2221delinsAG NP_009228.2:p.Glu740=
NM_007298.3:c.787+1574_787+1575delinsAG NP_009229.2:n.787+1574_787+1575delinsAG
NM_007299.3:c.787+1574_787+1575delinsAG NP_009230.2:n.787+1574_787+1575delinsAG
NM_007300.3:c.2361_2362delinsAG NP_009231.2:p.Glu787=
NR_027676.1:n.2497_2498delinsAG
NM_007294.4:c.2361_2362delinsAG MANE Select NP_009225.1:p.Glu787=
NM_007297.4:c.2220_2221delinsAG NP_009228.2:p.Glu740=
NM_007299.4:c.787+1574_787+1575delinsAG NP_009230.2:n.787+1574_787+1575delinsAG
NM_007300.4:c.2361_2362delinsAG NP_009231.2:p.Glu787=
NR_027676.2:n.2538_2539delinsAG