Canonical Allele Identifier: CA1139665621
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 936488
ClinVar RCV Id: RCV001205297
dbSNP Id: rs886038008

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43092517dup , CM000679.2:g.43092517dup GRCh38
NC_000017.10:g.41244534dup , CM000679.1:g.41244534dup GRCh37
NC_000017.9:g.38498060dup NCBI36
NG_005905.2:g.125468dup , LRG_292:g.125468dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.3079dup
ENST00000461574.2:c.3015dup ENSP00000417241.2:p.His1006ThrfsTer6
ENST00000470026.6:c.3015dup ENSP00000419274.2:p.His1006ThrfsTer6
ENST00000473961.6:c.2889dup ENSP00000420201.2:p.His964ThrfsTer6
ENST00000476777.6:c.3012dup ENSP00000417554.2:p.His1005ThrfsTer6
ENST00000477152.6:c.2937dup ENSP00000419988.2:p.His980ThrfsTer6
ENST00000478531.6:c.785-1484dup ENSP00000420412.2:n.785-1484dup
ENST00000489037.2:c.2937dup ENSP00000420781.2:p.His980ThrfsTer6
ENST00000493919.6:c.647-1484dup ENSP00000418819.2:n.647-1484dup
ENST00000494123.6:c.3015dup ENSP00000419103.2:p.His1006ThrfsTer6
ENST00000497488.2:c.2127dup ENSP00000418986.2:p.His710ThrfsTer6
ENST00000618469.2:c.3015dup ENSP00000478114.2:p.His1006ThrfsTer6
ENST00000634433.2:c.2892dup ENSP00000489431.2:p.His965ThrfsTer6
ENST00000644379.2:c.3015dup ENSP00000496570.2:p.His1006ThrfsTer6
ENST00000644555.2:c.647-1484dup ENSP00000494614.2:n.647-1484dup
ENST00000652672.2:c.2874dup ENSP00000498906.2:p.His959ThrfsTer6
ENST00000484087.6:c.665-1484dup ENSP00000419481.2:n.665-1484dup
ENST00000700182.1:c.707-1484dup ENSP00000514849.1:n.707-1484dup
ENST00000357654.9:c.3015dup MANE Select ENSP00000350283.3:p.His1006ThrfsTer6
ENST00000471181.7:c.3015dup ENSP00000418960.2:p.His1006ThrfsTer6
ENST00000352993.7:c.671-1484dup ENSP00000312236.5:n.671-1484dup
ENST00000354071.7:c.3015dup ENSP00000326002.7:p.His1006ThrfsTer6
ENST00000357654.7:c.3015dup ENSP00000350283.3:p.His1006ThrfsTer6
ENST00000461221.5:c.*2798dup ENSP00000418548.1:n.*2798dup
ENST00000468300.5:c.788-1484dup ENSP00000417148.1:n.788-1484dup
ENST00000471181.6:c.3015dup ENSP00000418960.2:p.His1006ThrfsTer6
ENST00000478531.5:c.785-1484dup ENSP00000420412.1:n.785-1484dup
ENST00000484087.5:c.410-1484dup ENSP00000419481.1:n.410-1484dup
ENST00000487825.5:c.413-1484dup ENSP00000418212.1:n.413-1484dup
ENST00000491747.6:c.788-1484dup ENSP00000420705.2:n.788-1484dup
ENST00000493795.5:c.2874dup ENSP00000418775.1:p.His959ThrfsTer6
ENST00000493919.5:c.647-1484dup ENSP00000418819.1:n.647-1484dup
ENST00000586385.5:c.5-28565dup ENSP00000465818.1:n.5-28565dup
ENST00000591534.5:c.-43-17995dup ENSP00000467329.1:n.-43-17995dup
ENST00000591849.5:c.-99+32755dup ENSP00000465347.1:n.-99+32755dup
NM_007294.3:c.3015dup , LRG_292t1:c.3015dup NP_009225.1:p.His1006ThrfsTer6
NM_007297.3:c.2874dup NP_009228.2:p.His959ThrfsTer6
NM_007298.3:c.788-1484dup NP_009229.2:n.788-1484dup
NM_007299.3:c.788-1484dup NP_009230.2:n.788-1484dup
NM_007300.3:c.3015dup NP_009231.2:p.His1006ThrfsTer6
NR_027676.1:n.3151dup
NM_007294.4:c.3015dup MANE Select NP_009225.1:p.His1006ThrfsTer6
NM_007297.4:c.2874dup NP_009228.2:p.His959ThrfsTer6
NM_007299.4:c.788-1484dup NP_009230.2:n.788-1484dup
NM_007300.4:c.3015dup NP_009231.2:p.His1006ThrfsTer6
NR_027676.2:n.3192dup