Canonical Allele Identifier: CA10589703
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 266429
dbSNP Id: rs886040187

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43091514_43091515insAA , CM000679.2:g.43091514_43091515insAA GRCh38
NC_000017.10:g.41243531_41243532insAA , CM000679.1:g.41243531_41243532insAA GRCh37
NC_000017.9:g.38497057_38497058insAA NCBI36
NG_005905.2:g.126469_126470insTT , LRG_292:g.126469_126470insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.4080_4081insTT
ENST00000461574.2:c.4016_4017insTT ENSP00000417241.2:p.Glu1339AspfsTer28
ENST00000470026.6:c.4016_4017insTT ENSP00000419274.2:p.Glu1339AspfsTer28
ENST00000473961.6:c.3890_3891insTT ENSP00000420201.2:p.Glu1297AspfsTer28
ENST00000476777.6:c.4013_4014insTT ENSP00000417554.2:p.Glu1338AspfsTer28
ENST00000477152.6:c.3938_3939insTT ENSP00000419988.2:p.Glu1313AspfsTer28
ENST00000478531.6:c.785-483_785-482insTT ENSP00000420412.2:n.785-483_785-482insTT
ENST00000489037.2:c.3938_3939insTT ENSP00000420781.2:p.Glu1313AspfsTer28
ENST00000493919.6:c.647-483_647-482insTT ENSP00000418819.2:n.647-483_647-482insTT
ENST00000494123.6:c.4016_4017insTT ENSP00000419103.2:p.Glu1339AspfsTer28
ENST00000497488.2:c.3128_3129insTT ENSP00000418986.2:p.Glu1043AspfsTer28
ENST00000618469.2:c.4016_4017insTT ENSP00000478114.2:p.Glu1339AspfsTer28
ENST00000634433.2:c.3893_3894insTT ENSP00000489431.2:p.Glu1298AspfsTer28
ENST00000644379.2:c.4016_4017insTT ENSP00000496570.2:p.Glu1339AspfsTer28
ENST00000644555.2:c.647-483_647-482insTT ENSP00000494614.2:n.647-483_647-482insTT
ENST00000652672.2:c.3875_3876insTT ENSP00000498906.2:p.Glu1292AspfsTer28
ENST00000484087.6:c.665-483_665-482insTT ENSP00000419481.2:n.665-483_665-482insTT
ENST00000700182.1:c.707-483_707-482insTT ENSP00000514849.1:n.707-483_707-482insTT
ENST00000357654.9:c.4016_4017insTT MANE Select ENSP00000350283.3:p.Glu1339AspfsTer28
ENST00000471181.7:c.4016_4017insTT ENSP00000418960.2:p.Glu1339AspfsTer28
ENST00000644379.1:c.337_338insTT
ENST00000352993.7:c.671-483_671-482insTT ENSP00000312236.5:n.671-483_671-482insTT
ENST00000354071.7:c.4016_4017insTT ENSP00000326002.7:p.Glu1339AspfsTer28
ENST00000357654.7:c.4016_4017insTT ENSP00000350283.3:p.Glu1339AspfsTer28
ENST00000461221.5:c.*3799_*3800insTT ENSP00000418548.1:n.*3799_*3800insTT
ENST00000461574.1:c.310_311insTT
ENST00000468300.5:c.788-483_788-482insTT ENSP00000417148.1:n.788-483_788-482insTT
ENST00000471181.6:c.4016_4017insTT ENSP00000418960.2:p.Glu1339AspfsTer28
ENST00000478531.5:c.785-483_785-482insTT ENSP00000420412.1:n.785-483_785-482insTT
ENST00000484087.5:c.410-483_410-482insTT ENSP00000419481.1:n.410-483_410-482insTT
ENST00000487825.5:c.413-483_413-482insTT ENSP00000418212.1:n.413-483_413-482insTT
ENST00000491747.6:c.788-483_788-482insTT ENSP00000420705.2:n.788-483_788-482insTT
ENST00000493795.5:c.3875_3876insTT ENSP00000418775.1:p.Glu1292AspfsTer28
ENST00000493919.5:c.647-483_647-482insTT ENSP00000418819.1:n.647-483_647-482insTT
ENST00000586385.5:c.5-27564_5-27563insTT ENSP00000465818.1:n.5-27564_5-27563insTT
ENST00000591534.5:c.-43-16994_-43-16993insTT ENSP00000467329.1:n.-43-16994_-43-16993insTT
ENST00000591849.5:c.-99+33756_-99+33757insTT ENSP00000465347.1:n.-99+33756_-99+33757insTT
NM_007294.3:c.4016_4017insTT , LRG_292t1:c.4016_4017insTT NP_009225.1:p.Glu1339AspfsTer28
NM_007297.3:c.3875_3876insTT NP_009228.2:p.Glu1292AspfsTer28
NM_007298.3:c.788-483_788-482insTT NP_009229.2:n.788-483_788-482insTT
NM_007299.3:c.788-483_788-482insTT NP_009230.2:n.788-483_788-482insTT
NM_007300.3:c.4016_4017insTT NP_009231.2:p.Glu1339AspfsTer28
NR_027676.1:n.4152_4153insTT
NM_007294.4:c.4016_4017insTT MANE Select NP_009225.1:p.Glu1339AspfsTer28
NM_007297.4:c.3875_3876insTT NP_009228.2:p.Glu1292AspfsTer28
NM_007299.4:c.788-483_788-482insTT NP_009230.2:n.788-483_788-482insTT
NM_007300.4:c.4016_4017insTT NP_009231.2:p.Glu1339AspfsTer28
NR_027676.2:n.4193_4194insTT