Canonical Allele Identifier: CA2499224476
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1071122
ClinVar RCV Id: RCV001383500
dbSNP Id: rs1555588074

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43092273_43092274insGCAA , CM000679.2:g.43092273_43092274insGCAA GRCh38
NC_000017.10:g.41244290_41244291insGCAA , CM000679.1:g.41244290_41244291insGCAA GRCh37
NC_000017.9:g.38497816_38497817insGCAA NCBI36
NG_005905.2:g.125710_125711insTTGC , LRG_292:g.125710_125711insTTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.3321_3322insTTGC
ENST00000461574.2:c.3257_3258insTTGC ENSP00000417241.2:p.Leu1086PhefsTer8
ENST00000470026.6:c.3257_3258insTTGC ENSP00000419274.2:p.Leu1086PhefsTer8
ENST00000473961.6:c.3131_3132insTTGC ENSP00000420201.2:p.Leu1044PhefsTer8
ENST00000476777.6:c.3254_3255insTTGC ENSP00000417554.2:p.Leu1085PhefsTer8
ENST00000477152.6:c.3179_3180insTTGC ENSP00000419988.2:p.Leu1060PhefsTer8
ENST00000478531.6:c.785-1242_785-1241insTTGC ENSP00000420412.2:n.785-1242_785-1241insTTGC
ENST00000489037.2:c.3179_3180insTTGC ENSP00000420781.2:p.Leu1060PhefsTer8
ENST00000493919.6:c.647-1242_647-1241insTTGC ENSP00000418819.2:n.647-1242_647-1241insTTGC
ENST00000494123.6:c.3257_3258insTTGC ENSP00000419103.2:p.Leu1086PhefsTer8
ENST00000497488.2:c.2369_2370insTTGC ENSP00000418986.2:p.Leu790PhefsTer8
ENST00000618469.2:c.3257_3258insTTGC ENSP00000478114.2:p.Leu1086PhefsTer8
ENST00000634433.2:c.3134_3135insTTGC ENSP00000489431.2:p.Leu1045PhefsTer8
ENST00000644379.2:c.3257_3258insTTGC ENSP00000496570.2:p.Leu1086PhefsTer8
ENST00000644555.2:c.647-1242_647-1241insTTGC ENSP00000494614.2:n.647-1242_647-1241insTTGC
ENST00000652672.2:c.3116_3117insTTGC ENSP00000498906.2:p.Leu1039PhefsTer8
ENST00000484087.6:c.665-1242_665-1241insTTGC ENSP00000419481.2:n.665-1242_665-1241insTTGC
ENST00000700182.1:c.707-1242_707-1241insTTGC ENSP00000514849.1:n.707-1242_707-1241insTTGC
ENST00000357654.9:c.3257_3258insTTGC MANE Select ENSP00000350283.3:p.Leu1086PhefsTer8
ENST00000471181.7:c.3257_3258insTTGC ENSP00000418960.2:p.Leu1086PhefsTer8
ENST00000352993.7:c.671-1242_671-1241insTTGC ENSP00000312236.5:n.671-1242_671-1241insTTGC
ENST00000354071.7:c.3257_3258insTTGC ENSP00000326002.7:p.Leu1086PhefsTer8
ENST00000357654.7:c.3257_3258insTTGC ENSP00000350283.3:p.Leu1086PhefsTer8
ENST00000461221.5:c.*3040_*3041insTTGC ENSP00000418548.1:n.*3040_*3041insTTGC
ENST00000468300.5:c.788-1242_788-1241insTTGC ENSP00000417148.1:n.788-1242_788-1241insTTGC
ENST00000471181.6:c.3257_3258insTTGC ENSP00000418960.2:p.Leu1086PhefsTer8
ENST00000478531.5:c.785-1242_785-1241insTTGC ENSP00000420412.1:n.785-1242_785-1241insTTGC
ENST00000484087.5:c.410-1242_410-1241insTTGC ENSP00000419481.1:n.410-1242_410-1241insTTGC
ENST00000487825.5:c.413-1242_413-1241insTTGC ENSP00000418212.1:n.413-1242_413-1241insTTGC
ENST00000491747.6:c.788-1242_788-1241insTTGC ENSP00000420705.2:n.788-1242_788-1241insTTGC
ENST00000493795.5:c.3116_3117insTTGC ENSP00000418775.1:p.Leu1039PhefsTer8
ENST00000493919.5:c.647-1242_647-1241insTTGC ENSP00000418819.1:n.647-1242_647-1241insTTGC
ENST00000586385.5:c.5-28323_5-28322insTTGC ENSP00000465818.1:n.5-28323_5-28322insTTGC
ENST00000591534.5:c.-43-17753_-43-17752insTTGC ENSP00000467329.1:n.-43-17753_-43-17752insTTGC
ENST00000591849.5:c.-99+32997_-99+32998insTTGC ENSP00000465347.1:n.-99+32997_-99+32998insTTGC
NM_007294.3:c.3257_3258insTTGC , LRG_292t1:c.3257_3258insTTGC NP_009225.1:p.Leu1086PhefsTer8
NM_007297.3:c.3116_3117insTTGC NP_009228.2:p.Leu1039PhefsTer8
NM_007298.3:c.788-1242_788-1241insTTGC NP_009229.2:n.788-1242_788-1241insTTGC
NM_007299.3:c.788-1242_788-1241insTTGC NP_009230.2:n.788-1242_788-1241insTTGC
NM_007300.3:c.3257_3258insTTGC NP_009231.2:p.Leu1086PhefsTer8
NR_027676.1:n.3393_3394insTTGC
NM_007294.4:c.3257_3258insTTGC MANE Select NP_009225.1:p.Leu1086PhefsTer8
NM_007297.4:c.3116_3117insTTGC NP_009228.2:p.Leu1039PhefsTer8
NM_007299.4:c.788-1242_788-1241insTTGC NP_009230.2:n.788-1242_788-1241insTTGC
NM_007300.4:c.3257_3258insTTGC NP_009231.2:p.Leu1086PhefsTer8
NR_027676.2:n.3434_3435insTTGC