Canonical Allele Identifier: CA2695200251
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2673993
ClinVar RCV Id: RCV003450594

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43115739_43115743delinsCTC , CM000679.2:g.43115739_43115743delinsCTC GRCh38
NC_000017.10:g.41267756_41267760delinsCTC , CM000679.1:g.41267756_41267760delinsCTC GRCh37
NC_000017.9:g.38521282_38521286delinsCTC NCBI36
NG_005905.2:g.102241_102245delinsGAG , LRG_292:g.102241_102245delinsGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.181_185delinsGAG
ENST00000461574.2:c.117_121delinsGAG ENSP00000417241.2:p.Cys39TrpfsTer26
ENST00000470026.6:c.117_121delinsGAG ENSP00000419274.2:p.Cys39TrpfsTer26
ENST00000473961.6:c.117_121delinsGAG ENSP00000420201.2:p.Cys39TrpfsTer26
ENST00000476777.6:c.117_121delinsGAG ENSP00000417554.2:p.Cys39TrpfsTer26
ENST00000477152.6:c.117_121delinsGAG ENSP00000419988.2:p.Cys39TrpfsTer15
ENST00000478531.6:c.117_121delinsGAG ENSP00000420412.2:p.Cys39TrpfsTer26
ENST00000489037.2:c.117_121delinsGAG ENSP00000420781.2:p.Cys39TrpfsTer15
ENST00000493919.6:c.-8+8274_-8+8278delinsGAG ENSP00000418819.2:n.-8+8274_-8+8278delinsGAG
ENST00000494123.6:c.117_121delinsGAG ENSP00000419103.2:p.Cys39TrpfsTer26
ENST00000497488.2:c.-219+9528_-219+9532delinsGAG ENSP00000418986.2:n.-219+9528_-219+9532delinsGAG
ENST00000618469.2:c.117_121delinsGAG ENSP00000478114.2:p.Cys39TrpfsTer26
ENST00000634433.2:c.117_121delinsGAG ENSP00000489431.2:p.Cys39TrpfsTer26
ENST00000644379.2:c.117_121delinsGAG ENSP00000496570.2:p.Cys39TrpfsTer26
ENST00000644555.2:c.-25_-21delinsGAG ENSP00000494614.2:n.-25_-21delinsGAG
ENST00000652672.2:c.-25_-21delinsGAG ENSP00000498906.2:n.-25_-21delinsGAG
ENST00000484087.6:c.117_121delinsGAG ENSP00000419481.2:p.Cys39TrpfsTer26
ENST00000700182.1:c.117_121delinsGAG ENSP00000514849.1:p.Cys39TrpfsTer15
ENST00000700183.1:c.117_121delinsGAG ENSP00000514850.1:p.Cys39TrpfsTer30
ENST00000700184.1:n.360_364delinsGAG
ENST00000700185.1:n.236_240delinsGAG
ENST00000357654.9:c.117_121delinsGAG MANE Select ENSP00000350283.3:p.Cys39TrpfsTer26
ENST00000471181.7:c.117_121delinsGAG ENSP00000418960.2:p.Cys39TrpfsTer26
ENST00000642945.1:c.117_121delinsGAG ENSP00000495897.1:p.Cys39TrpfsTer?
ENST00000644555.1:c.-25_-21delinsGAG ENSP00000494614.1:n.-25_-21delinsGAG
ENST00000652672.1:c.-25_-21delinsGAG ENSP00000498906.1:n.-25_-21delinsGAG
ENST00000352993.7:c.117_121delinsGAG ENSP00000312236.5:p.Cys39TrpfsTer26
ENST00000354071.7:c.117_121delinsGAG ENSP00000326002.7:p.Cys39TrpfsTer26
ENST00000357654.7:c.117_121delinsGAG ENSP00000350283.3:p.Cys39TrpfsTer26
ENST00000461221.5:c.117_121delinsGAG ENSP00000418548.1:p.Cys39TrpfsTer?
ENST00000461798.5:c.117_121delinsGAG ENSP00000417988.1:p.Cys39TrpfsTer?
ENST00000468300.5:c.117_121delinsGAG ENSP00000417148.1:p.Cys39TrpfsTer26
ENST00000470026.5:c.117_121delinsGAG ENSP00000419274.1:p.Cys39TrpfsTer26
ENST00000471181.6:c.117_121delinsGAG ENSP00000418960.2:p.Cys39TrpfsTer26
ENST00000476777.5:c.117_121delinsGAG ENSP00000417554.1:p.Cys39TrpfsTer26
ENST00000477152.5:c.117_121delinsGAG ENSP00000419988.1:p.Cys39TrpfsTer15
ENST00000478531.5:c.117_121delinsGAG ENSP00000420412.1:p.Cys39TrpfsTer26
ENST00000489037.1:c.117_121delinsGAG ENSP00000420781.1:p.Cys39TrpfsTer15
ENST00000491747.6:c.117_121delinsGAG ENSP00000420705.2:p.Cys39TrpfsTer26
ENST00000492859.5:c.117_121delinsGAG ENSP00000420253.1:p.Cys39TrpfsTer30
ENST00000493795.5:c.-8+8274_-8+8278delinsGAG ENSP00000418775.1:n.-8+8274_-8+8278delinsGAG
ENST00000493919.5:c.-8+8274_-8+8278delinsGAG ENSP00000418819.1:n.-8+8274_-8+8278delinsGAG
ENST00000494123.5:c.117_121delinsGAG ENSP00000419103.1:p.Cys39TrpfsTer26
ENST00000497488.1:c.-219+9528_-219+9532delinsGAG ENSP00000418986.1:n.-219+9528_-219+9532delinsGAG
ENST00000586385.5:c.4+9439_4+9443delinsGAG ENSP00000465818.1:n.4+9439_4+9443delinsGAG
ENST00000591534.5:c.-44+9528_-44+9532delinsGAG ENSP00000467329.1:n.-44+9528_-44+9532delinsGAG
ENST00000591849.5:c.-99+9528_-99+9532delinsGAG ENSP00000465347.1:n.-99+9528_-99+9532delinsGAG
ENST00000634433.1:c.117_121delinsGAG ENSP00000489431.1:p.Cys39TrpfsTer26
NM_007294.3:c.117_121delinsGAG , LRG_292t1:c.117_121delinsGAG NP_009225.1:p.Cys39TrpfsTer26
NM_007297.3:c.-8+8274_-8+8278delinsGAG NP_009228.2:n.-8+8274_-8+8278delinsGAG
NM_007298.3:c.117_121delinsGAG NP_009229.2:p.Cys39TrpfsTer26
NM_007299.3:c.117_121delinsGAG NP_009230.2:p.Cys39TrpfsTer26
NM_007300.3:c.117_121delinsGAG NP_009231.2:p.Cys39TrpfsTer26
NR_027676.1:n.278_282delinsGAG
NM_007294.4:c.117_121delinsGAG MANE Select NP_009225.1:p.Cys39TrpfsTer26
NM_007297.4:c.-8+8274_-8+8278delinsGAG NP_009228.2:n.-8+8274_-8+8278delinsGAG
NM_007299.4:c.117_121delinsGAG NP_009230.2:p.Cys39TrpfsTer26
NM_007300.4:c.117_121delinsGAG NP_009231.2:p.Cys39TrpfsTer26
NR_027676.2:n.319_323delinsGAG