Canonical Allele Identifier: CA2260782366
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43091864_43091867delinsGCTC , CM000679.2:g.43091864_43091867delinsGCTC GRCh38
NC_000017.10:g.41243881_41243884delinsGCTC , CM000679.1:g.41243881_41243884delinsGCTC GRCh37
NC_000017.9:g.38497407_38497410delinsGCTC NCBI36
NG_005905.2:g.126117_126120delinsGAGC , LRG_292:g.126117_126120delinsGAGC

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.3728_3731delinsGAGC
ENST00000461574.2:c.3664_3667delinsGAGC ENSP00000417241.2:p.Glu1222=
ENST00000470026.6:c.3664_3667delinsGAGC ENSP00000419274.2:p.Glu1222=
ENST00000473961.6:c.3538_3541delinsGAGC ENSP00000420201.2:p.Glu1180=
ENST00000476777.6:c.3661_3664delinsGAGC ENSP00000417554.2:p.Glu1221=
ENST00000477152.6:c.3586_3589delinsGAGC ENSP00000419988.2:p.Glu1196=
ENST00000478531.6:c.785-835_785-832delinsGAGC ENSP00000420412.2:n.785-835_785-832delinsGAGC
ENST00000489037.2:c.3586_3589delinsGAGC ENSP00000420781.2:p.Glu1196=
ENST00000493919.6:c.647-835_647-832delinsGAGC ENSP00000418819.2:n.647-835_647-832delinsGAGC
ENST00000494123.6:c.3664_3667delinsGAGC ENSP00000419103.2:p.Glu1222=
ENST00000497488.2:c.2776_2779delinsGAGC ENSP00000418986.2:p.Glu926=
ENST00000618469.2:c.3664_3667delinsGAGC ENSP00000478114.2:p.Glu1222=
ENST00000634433.2:c.3541_3544delinsGAGC ENSP00000489431.2:p.Glu1181=
ENST00000644379.2:c.3664_3667delinsGAGC ENSP00000496570.2:p.Glu1222=
ENST00000644555.2:c.647-835_647-832delinsGAGC ENSP00000494614.2:n.647-835_647-832delinsGAGC
ENST00000652672.2:c.3523_3526delinsGAGC ENSP00000498906.2:p.Glu1175=
ENST00000484087.6:c.665-835_665-832delinsGAGC ENSP00000419481.2:n.665-835_665-832delinsGAGC
ENST00000700182.1:c.707-835_707-832delinsGAGC ENSP00000514849.1:n.707-835_707-832delinsGAGC
ENST00000357654.9:c.3664_3667delinsGAGC MANE Select ENSP00000350283.3:p.Glu1222=
ENST00000471181.7:c.3664_3667delinsGAGC ENSP00000418960.2:p.Glu1222=
ENST00000352993.7:c.671-835_671-832delinsGAGC ENSP00000312236.5:n.671-835_671-832delinsGAGC
ENST00000354071.7:c.3664_3667delinsGAGC ENSP00000326002.7:p.Glu1222=
ENST00000357654.7:c.3664_3667delinsGAGC ENSP00000350283.3:p.Glu1222=
ENST00000461221.5:c.*3447_*3450delinsGAGC ENSP00000418548.1:n.*3447_*3450delinsGAGC
ENST00000468300.5:c.788-835_788-832delinsGAGC ENSP00000417148.1:n.788-835_788-832delinsGAGC
ENST00000471181.6:c.3664_3667delinsGAGC ENSP00000418960.2:p.Glu1222=
ENST00000478531.5:c.785-835_785-832delinsGAGC ENSP00000420412.1:n.785-835_785-832delinsGAGC
ENST00000484087.5:c.410-835_410-832delinsGAGC ENSP00000419481.1:n.410-835_410-832delinsGAGC
ENST00000487825.5:c.413-835_413-832delinsGAGC ENSP00000418212.1:n.413-835_413-832delinsGAGC
ENST00000491747.6:c.788-835_788-832delinsGAGC ENSP00000420705.2:n.788-835_788-832delinsGAGC
ENST00000493795.5:c.3523_3526delinsGAGC ENSP00000418775.1:p.Glu1175=
ENST00000493919.5:c.647-835_647-832delinsGAGC ENSP00000418819.1:n.647-835_647-832delinsGAGC
ENST00000586385.5:c.5-27916_5-27913delinsGAGC ENSP00000465818.1:n.5-27916_5-27913delinsGAGC
ENST00000591534.5:c.-43-17346_-43-17343delinsGAGC ENSP00000467329.1:n.-43-17346_-43-17343delinsGAGC
ENST00000591849.5:c.-99+33404_-99+33407delinsGAGC ENSP00000465347.1:n.-99+33404_-99+33407delinsGAGC
NM_007294.3:c.3664_3667delinsGAGC , LRG_292t1:c.3664_3667delinsGAGC NP_009225.1:p.Glu1222=
NM_007297.3:c.3523_3526delinsGAGC NP_009228.2:p.Glu1175=
NM_007298.3:c.788-835_788-832delinsGAGC NP_009229.2:n.788-835_788-832delinsGAGC
NM_007299.3:c.788-835_788-832delinsGAGC NP_009230.2:n.788-835_788-832delinsGAGC
NM_007300.3:c.3664_3667delinsGAGC NP_009231.2:p.Glu1222=
NR_027676.1:n.3800_3803delinsGAGC
NM_007294.4:c.3664_3667delinsGAGC MANE Select NP_009225.1:p.Glu1222=
NM_007297.4:c.3523_3526delinsGAGC NP_009228.2:p.Glu1175=
NM_007299.4:c.788-835_788-832delinsGAGC NP_009230.2:n.788-835_788-832delinsGAGC
NM_007300.4:c.3664_3667delinsGAGC NP_009231.2:p.Glu1222=
NR_027676.2:n.3841_3844delinsGAGC