Canonical Allele Identifier: CA2260790199
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43103931_43103932delinsAC , CM000679.2:g.43103931_43103932delinsAC GRCh38
NC_000017.10:g.41255948_41255949delinsAC , CM000679.1:g.41255948_41255949delinsAC GRCh37
NC_000017.9:g.38509474_38509475delinsAC NCBI36
NG_005905.2:g.114052_114053delinsGT , LRG_292:g.114052_114053delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.505+190_505+191delinsGT
ENST00000461574.2:c.441+190_441+191delinsGT ENSP00000417241.2:n.441+190_441+191delinsGT
ENST00000470026.6:c.441+190_441+191delinsGT ENSP00000419274.2:n.441+190_441+191delinsGT
ENST00000473961.6:c.441+190_441+191delinsGT ENSP00000420201.2:n.441+190_441+191delinsGT
ENST00000476777.6:c.441+190_441+191delinsGT ENSP00000417554.2:n.441+190_441+191delinsGT
ENST00000477152.6:c.363+190_363+191delinsGT ENSP00000419988.2:n.363+190_363+191delinsGT
ENST00000478531.6:c.441+190_441+191delinsGT ENSP00000420412.2:n.441+190_441+191delinsGT
ENST00000489037.2:c.363+190_363+191delinsGT ENSP00000420781.2:n.363+190_363+191delinsGT
ENST00000493919.6:c.300+190_300+191delinsGT ENSP00000418819.2:n.300+190_300+191delinsGT
ENST00000494123.6:c.441+190_441+191delinsGT ENSP00000419103.2:n.441+190_441+191delinsGT
ENST00000497488.2:c.-218-9072_-218-9071delinsGT ENSP00000418986.2:n.-218-9072_-218-9071delinsGT
ENST00000618469.2:c.441+190_441+191delinsGT ENSP00000478114.2:n.441+190_441+191delinsGT
ENST00000634433.2:c.441+190_441+191delinsGT ENSP00000489431.2:n.441+190_441+191delinsGT
ENST00000644379.2:c.441+190_441+191delinsGT ENSP00000496570.2:n.441+190_441+191delinsGT
ENST00000644555.2:c.300+190_300+191delinsGT ENSP00000494614.2:n.300+190_300+191delinsGT
ENST00000652672.2:c.300+190_300+191delinsGT ENSP00000498906.2:n.300+190_300+191delinsGT
ENST00000484087.6:c.441+190_441+191delinsGT ENSP00000419481.2:n.441+190_441+191delinsGT
ENST00000700182.1:c.363+190_363+191delinsGT ENSP00000514849.1:n.363+190_363+191delinsGT
ENST00000700183.1:c.*355+190_*355+191delinsGT ENSP00000514850.1:n.*355+190_*355+191delinsGT
ENST00000700184.1:n.684+190_684+191delinsGT
ENST00000357654.9:c.441+190_441+191delinsGT MANE Select ENSP00000350283.3:n.441+190_441+191delinsGT
ENST00000471181.7:c.441+190_441+191delinsGT ENSP00000418960.2:n.441+190_441+191delinsGT
ENST00000642945.1:c.*315+190_*315+191delinsGT ENSP00000495897.1:n.*315+190_*315+191delinsGT
ENST00000652672.1:c.300+190_300+191delinsGT ENSP00000498906.1:n.300+190_300+191delinsGT
ENST00000352993.7:c.441+190_441+191delinsGT ENSP00000312236.5:n.441+190_441+191delinsGT
ENST00000354071.7:c.441+190_441+191delinsGT ENSP00000326002.7:n.441+190_441+191delinsGT
ENST00000357654.7:c.441+190_441+191delinsGT ENSP00000350283.3:n.441+190_441+191delinsGT
ENST00000461221.5:c.*227+190_*227+191delinsGT ENSP00000418548.1:n.*227+190_*227+191delinsGT
ENST00000461798.5:c.*227+190_*227+191delinsGT ENSP00000417988.1:n.*227+190_*227+191delinsGT
ENST00000468300.5:c.441+190_441+191delinsGT ENSP00000417148.1:n.441+190_441+191delinsGT
ENST00000470026.5:c.441+190_441+191delinsGT ENSP00000419274.1:n.441+190_441+191delinsGT
ENST00000471181.6:c.441+190_441+191delinsGT ENSP00000418960.2:n.441+190_441+191delinsGT
ENST00000473961.5:c.164+190_164+191delinsGT
ENST00000476777.5:c.441+190_441+191delinsGT ENSP00000417554.1:n.441+190_441+191delinsGT
ENST00000477152.5:c.363+190_363+191delinsGT ENSP00000419988.1:n.363+190_363+191delinsGT
ENST00000478531.5:c.441+190_441+191delinsGT ENSP00000420412.1:n.441+190_441+191delinsGT
ENST00000484087.5:c.189+190_189+191delinsGT ENSP00000419481.1:n.189+190_189+191delinsGT
ENST00000487825.5:c.189+190_189+191delinsGT ENSP00000418212.1:n.189+190_189+191delinsGT
ENST00000491747.6:c.441+190_441+191delinsGT ENSP00000420705.2:n.441+190_441+191delinsGT
ENST00000492859.5:c.*377+190_*377+191delinsGT ENSP00000420253.1:n.*377+190_*377+191delinsGT
ENST00000493795.5:c.300+190_300+191delinsGT ENSP00000418775.1:n.300+190_300+191delinsGT
ENST00000493919.5:c.300+190_300+191delinsGT ENSP00000418819.1:n.300+190_300+191delinsGT
ENST00000494123.5:c.441+190_441+191delinsGT ENSP00000419103.1:n.441+190_441+191delinsGT
ENST00000497488.1:c.-218-9072_-218-9071delinsGT ENSP00000418986.1:n.-218-9072_-218-9071delinsGT
ENST00000586385.5:c.4+21250_4+21251delinsGT ENSP00000465818.1:n.4+21250_4+21251delinsGT
ENST00000591534.5:c.-44+21339_-44+21340delinsGT ENSP00000467329.1:n.-44+21339_-44+21340delinsGT
ENST00000591849.5:c.-99+21339_-99+21340delinsGT ENSP00000465347.1:n.-99+21339_-99+21340delinsGT
ENST00000634433.1:c.441+190_441+191delinsGT ENSP00000489431.1:n.441+190_441+191delinsGT
NM_007294.3:c.441+190_441+191delinsGT , LRG_292t1:c.441+190_441+191delinsGT NP_009225.1:n.441+190_441+191delinsGT
NM_007297.3:c.300+190_300+191delinsGT NP_009228.2:n.300+190_300+191delinsGT
NM_007298.3:c.441+190_441+191delinsGT NP_009229.2:n.441+190_441+191delinsGT
NM_007299.3:c.441+190_441+191delinsGT NP_009230.2:n.441+190_441+191delinsGT
NM_007300.3:c.441+190_441+191delinsGT NP_009231.2:n.441+190_441+191delinsGT
NR_027676.1:n.580+190_580+191delinsGT
NM_007294.4:c.441+190_441+191delinsGT MANE Select NP_009225.1:n.441+190_441+191delinsGT
NM_007297.4:c.300+190_300+191delinsGT NP_009228.2:n.300+190_300+191delinsGT
NM_007299.4:c.441+190_441+191delinsGT NP_009230.2:n.441+190_441+191delinsGT
NM_007300.4:c.441+190_441+191delinsGT NP_009231.2:n.441+190_441+191delinsGT
NR_027676.2:n.621+190_621+191delinsGT