Canonical Allele Identifier: CA2580617965
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2580193
ClinVar RCV Id: RCV003329158

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43092278_43092279insTT , CM000679.2:g.43092278_43092279insTT GRCh38
NC_000017.10:g.41244295_41244296insTT , CM000679.1:g.41244295_41244296insTT GRCh37
NC_000017.9:g.38497821_38497822insTT NCBI36
NG_005905.2:g.125706_125707insAA , LRG_292:g.125706_125707insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.3317_3318insAA
ENST00000461574.2:c.3253_3254insAA ENSP00000417241.2:p.Arg1085LysfsTer3
ENST00000470026.6:c.3253_3254insAA ENSP00000419274.2:p.Arg1085LysfsTer3
ENST00000473961.6:c.3127_3128insAA ENSP00000420201.2:p.Arg1043LysfsTer3
ENST00000476777.6:c.3250_3251insAA ENSP00000417554.2:p.Arg1084LysfsTer3
ENST00000477152.6:c.3175_3176insAA ENSP00000419988.2:p.Arg1059LysfsTer3
ENST00000478531.6:c.785-1246_785-1245insAA ENSP00000420412.2:n.785-1246_785-1245insAA
ENST00000489037.2:c.3175_3176insAA ENSP00000420781.2:p.Arg1059LysfsTer3
ENST00000493919.6:c.647-1246_647-1245insAA ENSP00000418819.2:n.647-1246_647-1245insAA
ENST00000494123.6:c.3253_3254insAA ENSP00000419103.2:p.Arg1085LysfsTer3
ENST00000497488.2:c.2365_2366insAA ENSP00000418986.2:p.Arg789LysfsTer3
ENST00000618469.2:c.3253_3254insAA ENSP00000478114.2:p.Arg1085LysfsTer3
ENST00000634433.2:c.3130_3131insAA ENSP00000489431.2:p.Arg1044LysfsTer3
ENST00000644379.2:c.3253_3254insAA ENSP00000496570.2:p.Arg1085LysfsTer3
ENST00000644555.2:c.647-1246_647-1245insAA ENSP00000494614.2:n.647-1246_647-1245insAA
ENST00000652672.2:c.3112_3113insAA ENSP00000498906.2:p.Arg1038LysfsTer3
ENST00000484087.6:c.665-1246_665-1245insAA ENSP00000419481.2:n.665-1246_665-1245insAA
ENST00000700182.1:c.707-1246_707-1245insAA ENSP00000514849.1:n.707-1246_707-1245insAA
ENST00000357654.9:c.3253_3254insAA MANE Select ENSP00000350283.3:p.Arg1085LysfsTer3
ENST00000471181.7:c.3253_3254insAA ENSP00000418960.2:p.Arg1085LysfsTer3
ENST00000352993.7:c.671-1246_671-1245insAA ENSP00000312236.5:n.671-1246_671-1245insAA
ENST00000354071.7:c.3253_3254insAA ENSP00000326002.7:p.Arg1085LysfsTer3
ENST00000357654.7:c.3253_3254insAA ENSP00000350283.3:p.Arg1085LysfsTer3
ENST00000461221.5:c.*3036_*3037insAA ENSP00000418548.1:n.*3036_*3037insAA
ENST00000468300.5:c.788-1246_788-1245insAA ENSP00000417148.1:n.788-1246_788-1245insAA
ENST00000471181.6:c.3253_3254insAA ENSP00000418960.2:p.Arg1085LysfsTer3
ENST00000478531.5:c.785-1246_785-1245insAA ENSP00000420412.1:n.785-1246_785-1245insAA
ENST00000484087.5:c.410-1246_410-1245insAA ENSP00000419481.1:n.410-1246_410-1245insAA
ENST00000487825.5:c.413-1246_413-1245insAA ENSP00000418212.1:n.413-1246_413-1245insAA
ENST00000491747.6:c.788-1246_788-1245insAA ENSP00000420705.2:n.788-1246_788-1245insAA
ENST00000493795.5:c.3112_3113insAA ENSP00000418775.1:p.Arg1038LysfsTer3
ENST00000493919.5:c.647-1246_647-1245insAA ENSP00000418819.1:n.647-1246_647-1245insAA
ENST00000586385.5:c.5-28327_5-28326insAA ENSP00000465818.1:n.5-28327_5-28326insAA
ENST00000591534.5:c.-43-17757_-43-17756insAA ENSP00000467329.1:n.-43-17757_-43-17756insAA
ENST00000591849.5:c.-99+32993_-99+32994insAA ENSP00000465347.1:n.-99+32993_-99+32994insAA
NM_007294.3:c.3253_3254insAA , LRG_292t1:c.3253_3254insAA NP_009225.1:p.Arg1085LysfsTer3
NM_007297.3:c.3112_3113insAA NP_009228.2:p.Arg1038LysfsTer3
NM_007298.3:c.788-1246_788-1245insAA NP_009229.2:n.788-1246_788-1245insAA
NM_007299.3:c.788-1246_788-1245insAA NP_009230.2:n.788-1246_788-1245insAA
NM_007300.3:c.3253_3254insAA NP_009231.2:p.Arg1085LysfsTer3
NR_027676.1:n.3389_3390insAA
NM_007294.4:c.3253_3254insAA MANE Select NP_009225.1:p.Arg1085LysfsTer3
NM_007297.4:c.3112_3113insAA NP_009228.2:p.Arg1038LysfsTer3
NM_007299.4:c.788-1246_788-1245insAA NP_009230.2:n.788-1246_788-1245insAA
NM_007300.4:c.3253_3254insAA NP_009231.2:p.Arg1085LysfsTer3
NR_027676.2:n.3430_3431insAA