Canonical Allele Identifier: CA658825032
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 548195
ClinVar RCV Id: RCV000661006
dbSNP Id: rs1555586564

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43091479_43091480insC , CM000679.2:g.43091479_43091480insC GRCh38
NC_000017.10:g.41243496_41243497insC , CM000679.1:g.41243496_41243497insC GRCh37
NC_000017.9:g.38497022_38497023insC NCBI36
NG_005905.2:g.126504_126505insG , LRG_292:g.126504_126505insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.4115_4116insG
ENST00000461574.2:c.4051_4052insG ENSP00000417241.2:p.Leu1351CysfsTer5
ENST00000470026.6:c.4051_4052insG ENSP00000419274.2:p.Leu1351CysfsTer5
ENST00000473961.6:c.3925_3926insG ENSP00000420201.2:p.Leu1309CysfsTer5
ENST00000476777.6:c.4048_4049insG ENSP00000417554.2:p.Leu1350CysfsTer5
ENST00000477152.6:c.3973_3974insG ENSP00000419988.2:p.Leu1325CysfsTer5
ENST00000478531.6:c.785-448_785-447insG ENSP00000420412.2:n.785-448_785-447insG
ENST00000489037.2:c.3973_3974insG ENSP00000420781.2:p.Leu1325CysfsTer5
ENST00000493919.6:c.647-448_647-447insG ENSP00000418819.2:n.647-448_647-447insG
ENST00000494123.6:c.4051_4052insG ENSP00000419103.2:p.Leu1351CysfsTer5
ENST00000497488.2:c.3163_3164insG ENSP00000418986.2:p.Leu1055CysfsTer5
ENST00000618469.2:c.4051_4052insG ENSP00000478114.2:p.Leu1351CysfsTer5
ENST00000634433.2:c.3928_3929insG ENSP00000489431.2:p.Leu1310CysfsTer5
ENST00000644379.2:c.4051_4052insG ENSP00000496570.2:p.Leu1351CysfsTer5
ENST00000644555.2:c.647-448_647-447insG ENSP00000494614.2:n.647-448_647-447insG
ENST00000652672.2:c.3910_3911insG ENSP00000498906.2:p.Leu1304CysfsTer5
ENST00000484087.6:c.665-448_665-447insG ENSP00000419481.2:n.665-448_665-447insG
ENST00000700182.1:c.707-448_707-447insG ENSP00000514849.1:n.707-448_707-447insG
ENST00000357654.9:c.4051_4052insG MANE Select ENSP00000350283.3:p.Leu1351CysfsTer5
ENST00000471181.7:c.4051_4052insG ENSP00000418960.2:p.Leu1351CysfsTer5
ENST00000644379.1:c.372_373insG
ENST00000352993.7:c.671-448_671-447insG ENSP00000312236.5:n.671-448_671-447insG
ENST00000354071.7:c.4051_4052insG ENSP00000326002.7:p.Leu1351CysfsTer5
ENST00000357654.7:c.4051_4052insG ENSP00000350283.3:p.Leu1351CysfsTer5
ENST00000461221.5:c.*3834_*3835insG ENSP00000418548.1:n.*3834_*3835insG
ENST00000461574.1:c.345_346insG
ENST00000468300.5:c.788-448_788-447insG ENSP00000417148.1:n.788-448_788-447insG
ENST00000471181.6:c.4051_4052insG ENSP00000418960.2:p.Leu1351CysfsTer5
ENST00000478531.5:c.785-448_785-447insG ENSP00000420412.1:n.785-448_785-447insG
ENST00000484087.5:c.410-448_410-447insG ENSP00000419481.1:n.410-448_410-447insG
ENST00000487825.5:c.413-448_413-447insG ENSP00000418212.1:n.413-448_413-447insG
ENST00000491747.6:c.788-448_788-447insG ENSP00000420705.2:n.788-448_788-447insG
ENST00000493795.5:c.3910_3911insG ENSP00000418775.1:p.Leu1304CysfsTer5
ENST00000493919.5:c.647-448_647-447insG ENSP00000418819.1:n.647-448_647-447insG
ENST00000586385.5:c.5-27529_5-27528insG ENSP00000465818.1:n.5-27529_5-27528insG
ENST00000591534.5:c.-43-16959_-43-16958insG ENSP00000467329.1:n.-43-16959_-43-16958insG
ENST00000591849.5:c.-99+33791_-99+33792insG ENSP00000465347.1:n.-99+33791_-99+33792insG
NM_007294.3:c.4051_4052insG , LRG_292t1:c.4051_4052insG NP_009225.1:p.Leu1351CysfsTer5
NM_007297.3:c.3910_3911insG NP_009228.2:p.Leu1304CysfsTer5
NM_007298.3:c.788-448_788-447insG NP_009229.2:n.788-448_788-447insG
NM_007299.3:c.788-448_788-447insG NP_009230.2:n.788-448_788-447insG
NM_007300.3:c.4051_4052insG NP_009231.2:p.Leu1351CysfsTer5
NR_027676.1:n.4187_4188insG
NM_007294.4:c.4051_4052insG MANE Select NP_009225.1:p.Leu1351CysfsTer5
NM_007297.4:c.3910_3911insG NP_009228.2:p.Leu1304CysfsTer5
NM_007299.4:c.788-448_788-447insG NP_009230.2:n.788-448_788-447insG
NM_007300.4:c.4051_4052insG NP_009231.2:p.Leu1351CysfsTer5
NR_027676.2:n.4228_4229insG