Canonical Allele Identifier: CA2260782780
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43092274_43092276delinsAAT , CM000679.2:g.43092274_43092276delinsAAT GRCh38
NC_000017.10:g.41244291_41244293delinsAAT , CM000679.1:g.41244291_41244293delinsAAT GRCh37
NC_000017.9:g.38497817_38497819delinsAAT NCBI36
NG_005905.2:g.125708_125710delinsATT , LRG_292:g.125708_125710delinsATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.3319_3321delinsATT
ENST00000461574.2:c.3255_3257delinsATT ENSP00000417241.2:p.Arg1085=
ENST00000470026.6:c.3255_3257delinsATT ENSP00000419274.2:p.Arg1085=
ENST00000473961.6:c.3129_3131delinsATT ENSP00000420201.2:p.Arg1043=
ENST00000476777.6:c.3252_3254delinsATT ENSP00000417554.2:p.Arg1084=
ENST00000477152.6:c.3177_3179delinsATT ENSP00000419988.2:p.Arg1059=
ENST00000478531.6:c.785-1244_785-1242delinsATT ENSP00000420412.2:n.785-1244_785-1242delinsATT
ENST00000489037.2:c.3177_3179delinsATT ENSP00000420781.2:p.Arg1059=
ENST00000493919.6:c.647-1244_647-1242delinsATT ENSP00000418819.2:n.647-1244_647-1242delinsATT
ENST00000494123.6:c.3255_3257delinsATT ENSP00000419103.2:p.Arg1085=
ENST00000497488.2:c.2367_2369delinsATT ENSP00000418986.2:p.Arg789=
ENST00000618469.2:c.3255_3257delinsATT ENSP00000478114.2:p.Arg1085=
ENST00000634433.2:c.3132_3134delinsATT ENSP00000489431.2:p.Arg1044=
ENST00000644379.2:c.3255_3257delinsATT ENSP00000496570.2:p.Arg1085=
ENST00000644555.2:c.647-1244_647-1242delinsATT ENSP00000494614.2:n.647-1244_647-1242delinsATT
ENST00000652672.2:c.3114_3116delinsATT ENSP00000498906.2:p.Arg1038=
ENST00000484087.6:c.665-1244_665-1242delinsATT ENSP00000419481.2:n.665-1244_665-1242delinsATT
ENST00000700182.1:c.707-1244_707-1242delinsATT ENSP00000514849.1:n.707-1244_707-1242delinsATT
ENST00000357654.9:c.3255_3257delinsATT MANE Select ENSP00000350283.3:p.Arg1085=
ENST00000471181.7:c.3255_3257delinsATT ENSP00000418960.2:p.Arg1085=
ENST00000352993.7:c.671-1244_671-1242delinsATT ENSP00000312236.5:n.671-1244_671-1242delinsATT
ENST00000354071.7:c.3255_3257delinsATT ENSP00000326002.7:p.Arg1085=
ENST00000357654.7:c.3255_3257delinsATT ENSP00000350283.3:p.Arg1085=
ENST00000461221.5:c.*3038_*3040delinsATT ENSP00000418548.1:n.*3038_*3040delinsATT
ENST00000468300.5:c.788-1244_788-1242delinsATT ENSP00000417148.1:n.788-1244_788-1242delinsATT
ENST00000471181.6:c.3255_3257delinsATT ENSP00000418960.2:p.Arg1085=
ENST00000478531.5:c.785-1244_785-1242delinsATT ENSP00000420412.1:n.785-1244_785-1242delinsATT
ENST00000484087.5:c.410-1244_410-1242delinsATT ENSP00000419481.1:n.410-1244_410-1242delinsATT
ENST00000487825.5:c.413-1244_413-1242delinsATT ENSP00000418212.1:n.413-1244_413-1242delinsATT
ENST00000491747.6:c.788-1244_788-1242delinsATT ENSP00000420705.2:n.788-1244_788-1242delinsATT
ENST00000493795.5:c.3114_3116delinsATT ENSP00000418775.1:p.Arg1038=
ENST00000493919.5:c.647-1244_647-1242delinsATT ENSP00000418819.1:n.647-1244_647-1242delinsATT
ENST00000586385.5:c.5-28325_5-28323delinsATT ENSP00000465818.1:n.5-28325_5-28323delinsATT
ENST00000591534.5:c.-43-17755_-43-17753delinsATT ENSP00000467329.1:n.-43-17755_-43-17753delinsATT
ENST00000591849.5:c.-99+32995_-99+32997delinsATT ENSP00000465347.1:n.-99+32995_-99+32997delinsATT
NM_007294.3:c.3255_3257delinsATT , LRG_292t1:c.3255_3257delinsATT NP_009225.1:p.Arg1085=
NM_007297.3:c.3114_3116delinsATT NP_009228.2:p.Arg1038=
NM_007298.3:c.788-1244_788-1242delinsATT NP_009229.2:n.788-1244_788-1242delinsATT
NM_007299.3:c.788-1244_788-1242delinsATT NP_009230.2:n.788-1244_788-1242delinsATT
NM_007300.3:c.3255_3257delinsATT NP_009231.2:p.Arg1085=
NR_027676.1:n.3391_3393delinsATT
NM_007294.4:c.3255_3257delinsATT MANE Select NP_009225.1:p.Arg1085=
NM_007297.4:c.3114_3116delinsATT NP_009228.2:p.Arg1038=
NM_007299.4:c.788-1244_788-1242delinsATT NP_009230.2:n.788-1244_788-1242delinsATT
NM_007300.4:c.3255_3257delinsATT NP_009231.2:p.Arg1085=
NR_027676.2:n.3432_3434delinsATT