Canonical Allele Identifier: CA2260781948
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43091465_43091468delinsGATT , CM000679.2:g.43091465_43091468delinsGATT GRCh38
NC_000017.10:g.41243482_41243485delinsGATT , CM000679.1:g.41243482_41243485delinsGATT GRCh37
NC_000017.9:g.38497008_38497011delinsGATT NCBI36
NG_005905.2:g.126516_126519delinsAATC , LRG_292:g.126516_126519delinsAATC

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.4127_4130delinsAATC
ENST00000461574.2:c.4063_4066delinsAATC ENSP00000417241.2:p.Asn1355=
ENST00000470026.6:c.4063_4066delinsAATC ENSP00000419274.2:p.Asn1355=
ENST00000473961.6:c.3937_3940delinsAATC ENSP00000420201.2:p.Asn1313=
ENST00000476777.6:c.4060_4063delinsAATC ENSP00000417554.2:p.Asn1354=
ENST00000477152.6:c.3985_3988delinsAATC ENSP00000419988.2:p.Asn1329=
ENST00000478531.6:c.785-436_785-433delinsAATC ENSP00000420412.2:n.785-436_785-433delinsAATC
ENST00000489037.2:c.3985_3988delinsAATC ENSP00000420781.2:p.Asn1329=
ENST00000493919.6:c.647-436_647-433delinsAATC ENSP00000418819.2:n.647-436_647-433delinsAATC
ENST00000494123.6:c.4063_4066delinsAATC ENSP00000419103.2:p.Asn1355=
ENST00000497488.2:c.3175_3178delinsAATC ENSP00000418986.2:p.Asn1059=
ENST00000618469.2:c.4063_4066delinsAATC ENSP00000478114.2:p.Asn1355=
ENST00000634433.2:c.3940_3943delinsAATC ENSP00000489431.2:p.Asn1314=
ENST00000644379.2:c.4063_4066delinsAATC ENSP00000496570.2:p.Asn1355=
ENST00000644555.2:c.647-436_647-433delinsAATC ENSP00000494614.2:n.647-436_647-433delinsAATC
ENST00000652672.2:c.3922_3925delinsAATC ENSP00000498906.2:p.Asn1308=
ENST00000484087.6:c.665-436_665-433delinsAATC ENSP00000419481.2:n.665-436_665-433delinsAATC
ENST00000700182.1:c.707-436_707-433delinsAATC ENSP00000514849.1:n.707-436_707-433delinsAATC
ENST00000357654.9:c.4063_4066delinsAATC MANE Select ENSP00000350283.3:p.Asn1355=
ENST00000471181.7:c.4063_4066delinsAATC ENSP00000418960.2:p.Asn1355=
ENST00000644379.1:c.384_387delinsAATC
ENST00000352993.7:c.671-436_671-433delinsAATC ENSP00000312236.5:n.671-436_671-433delinsAATC
ENST00000354071.7:c.4063_4066delinsAATC ENSP00000326002.7:p.Asn1355=
ENST00000357654.7:c.4063_4066delinsAATC ENSP00000350283.3:p.Asn1355=
ENST00000461221.5:c.*3846_*3849delinsAATC ENSP00000418548.1:n.*3846_*3849delinsAATC
ENST00000461574.1:c.357_360delinsAATC
ENST00000468300.5:c.788-436_788-433delinsAATC ENSP00000417148.1:n.788-436_788-433delinsAATC
ENST00000471181.6:c.4063_4066delinsAATC ENSP00000418960.2:p.Asn1355=
ENST00000478531.5:c.785-436_785-433delinsAATC ENSP00000420412.1:n.785-436_785-433delinsAATC
ENST00000484087.5:c.410-436_410-433delinsAATC ENSP00000419481.1:n.410-436_410-433delinsAATC
ENST00000487825.5:c.413-436_413-433delinsAATC ENSP00000418212.1:n.413-436_413-433delinsAATC
ENST00000491747.6:c.788-436_788-433delinsAATC ENSP00000420705.2:n.788-436_788-433delinsAATC
ENST00000493795.5:c.3922_3925delinsAATC ENSP00000418775.1:p.Asn1308=
ENST00000493919.5:c.647-436_647-433delinsAATC ENSP00000418819.1:n.647-436_647-433delinsAATC
ENST00000586385.5:c.5-27517_5-27514delinsAATC ENSP00000465818.1:n.5-27517_5-27514delinsAATC
ENST00000591534.5:c.-43-16947_-43-16944delinsAATC ENSP00000467329.1:n.-43-16947_-43-16944delinsAATC
ENST00000591849.5:c.-99+33803_-99+33806delinsAATC ENSP00000465347.1:n.-99+33803_-99+33806delinsAATC
NM_007294.3:c.4063_4066delinsAATC , LRG_292t1:c.4063_4066delinsAATC NP_009225.1:p.Asn1355=
NM_007297.3:c.3922_3925delinsAATC NP_009228.2:p.Asn1308=
NM_007298.3:c.788-436_788-433delinsAATC NP_009229.2:n.788-436_788-433delinsAATC
NM_007299.3:c.788-436_788-433delinsAATC NP_009230.2:n.788-436_788-433delinsAATC
NM_007300.3:c.4063_4066delinsAATC NP_009231.2:p.Asn1355=
NR_027676.1:n.4199_4202delinsAATC
NM_007294.4:c.4063_4066delinsAATC MANE Select NP_009225.1:p.Asn1355=
NM_007297.4:c.3922_3925delinsAATC NP_009228.2:p.Asn1308=
NM_007299.4:c.788-436_788-433delinsAATC NP_009230.2:n.788-436_788-433delinsAATC
NM_007300.4:c.4063_4066delinsAATC NP_009231.2:p.Asn1355=
NR_027676.2:n.4240_4243delinsAATC