Canonical Allele Identifier: CA2260782133
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43091656_43091657delinsGA , CM000679.2:g.43091656_43091657delinsGA GRCh38
NC_000017.10:g.41243673_41243674delinsGA , CM000679.1:g.41243673_41243674delinsGA GRCh37
NC_000017.9:g.38497199_38497200delinsGA NCBI36
NG_005905.2:g.126327_126328delinsTC , LRG_292:g.126327_126328delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.3938_3939delinsTC
ENST00000461574.2:c.3874_3875delinsTC ENSP00000417241.2:p.Ser1292=
ENST00000470026.6:c.3874_3875delinsTC ENSP00000419274.2:p.Ser1292=
ENST00000473961.6:c.3748_3749delinsTC ENSP00000420201.2:p.Ser1250=
ENST00000476777.6:c.3871_3872delinsTC ENSP00000417554.2:p.Ser1291=
ENST00000477152.6:c.3796_3797delinsTC ENSP00000419988.2:p.Ser1266=
ENST00000478531.6:c.785-625_785-624delinsTC ENSP00000420412.2:n.785-625_785-624delins...
ENST00000489037.2:c.3796_3797delinsTC ENSP00000420781.2:p.Ser1266=
ENST00000493919.6:c.647-625_647-624delinsTC ENSP00000418819.2:n.647-625_647-624delins...
ENST00000494123.6:c.3874_3875delinsTC ENSP00000419103.2:p.Ser1292=
ENST00000497488.2:c.2986_2987delinsTC ENSP00000418986.2:p.Ser996=
ENST00000618469.2:c.3874_3875delinsTC ENSP00000478114.2:p.Ser1292=
ENST00000634433.2:c.3751_3752delinsTC ENSP00000489431.2:p.Ser1251=
ENST00000644379.2:c.3874_3875delinsTC ENSP00000496570.2:p.Ser1292=
ENST00000644555.2:c.647-625_647-624delinsTC ENSP00000494614.2:n.647-625_647-624delins...
ENST00000652672.2:c.3733_3734delinsTC ENSP00000498906.2:p.Ser1245=
ENST00000484087.6:c.665-625_665-624delinsTC ENSP00000419481.2:n.665-625_665-624delins...
ENST00000700182.1:c.707-625_707-624delinsTC ENSP00000514849.1:n.707-625_707-624delins...
ENST00000357654.9:c.3874_3875delinsTC MANE Select ENSP00000350283.3:p.Ser1292=
ENST00000471181.7:c.3874_3875delinsTC ENSP00000418960.2:p.Ser1292=
ENST00000644379.1:c.195_196delinsTC
ENST00000352993.7:c.671-625_671-624delinsTC ENSP00000312236.5:n.671-625_671-624delins...
ENST00000354071.7:c.3874_3875delinsTC ENSP00000326002.7:p.Ser1292=
ENST00000357654.7:c.3874_3875delinsTC ENSP00000350283.3:p.Ser1292=
ENST00000461221.5:c.*3657_*3658delinsTC ENSP00000418548.1:n.*3657_*3658delinsTC
ENST00000461574.1:c.168_169delinsTC
ENST00000468300.5:c.788-625_788-624delinsTC ENSP00000417148.1:n.788-625_788-624delins...
ENST00000471181.6:c.3874_3875delinsTC ENSP00000418960.2:p.Ser1292=
ENST00000478531.5:c.785-625_785-624delinsTC ENSP00000420412.1:n.785-625_785-624delins...
ENST00000484087.5:c.410-625_410-624delinsTC ENSP00000419481.1:n.410-625_410-624delins...
ENST00000487825.5:c.413-625_413-624delinsTC ENSP00000418212.1:n.413-625_413-624delins...
ENST00000491747.6:c.788-625_788-624delinsTC ENSP00000420705.2:n.788-625_788-624delins...
ENST00000493795.5:c.3733_3734delinsTC ENSP00000418775.1:p.Ser1245=
ENST00000493919.5:c.647-625_647-624delinsTC ENSP00000418819.1:n.647-625_647-624delins...
ENST00000586385.5:c.5-27706_5-27705delinsTC ENSP00000465818.1:n.5-27706_5-27705delins...
ENST00000591534.5:c.-43-17136_-43-17135delinsTC ENSP00000467329.1:n.-43-17136_-43-17135de...
ENST00000591849.5:c.-99+33614_-99+33615delinsTC ENSP00000465347.1:n.-99+33614_-99+33615de...
NM_007294.3:c.3874_3875delinsTC , LRG_292t1:c.3874_3875delinsTC NP_009225.1:p.Ser1292=
NM_007297.3:c.3733_3734delinsTC NP_009228.2:p.Ser1245=
NM_007298.3:c.788-625_788-624delinsTC NP_009229.2:n.788-625_788-624delinsTC
NM_007299.3:c.788-625_788-624delinsTC NP_009230.2:n.788-625_788-624delinsTC
NM_007300.3:c.3874_3875delinsTC NP_009231.2:p.Ser1292=
NR_027676.1:n.4010_4011delinsTC
NM_007294.4:c.3874_3875delinsTC MANE Select NP_009225.1:p.Ser1292=
NM_007297.4:c.3733_3734delinsTC NP_009228.2:p.Ser1245=
NM_007299.4:c.788-625_788-624delinsTC NP_009230.2:n.788-625_788-624delinsTC
NM_007300.4:c.3874_3875delinsTC NP_009231.2:p.Ser1292=
NR_027676.2:n.4051_4052delinsTC