Canonical Allele Identifier: CA2260761114
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43045763_43045774delinsTCTCGGGTCACC , CM000679.2:g.43045763_43045774delinsTCTCGGGTCACC GRCh38
NC_000017.10:g.41197780_41197791delinsTCTCGGGTCACC , CM000679.1:g.41197780_41197791delinsTCTCGGGTCACC GRCh37
NC_000017.9:g.38451306_38451317delinsTCTCGGGTCACC NCBI36
NG_005905.2:g.172210_172221delinsGGTGACCCGAGA , LRG_292:g.172210_172221delinsGGTGACCCGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5493_5504delinsGGTGACCCGAGA ENSP00000417241.2:p.Val1831=
ENST00000470026.6:c.5496_5507delinsGGTGACCCGAGA ENSP00000419274.2:p.Val1832=
ENST00000473961.6:c.5370_5381delinsGGTGACCCGAGA ENSP00000420201.2:p.Val1790=
ENST00000476777.6:c.5490_5501delinsGGTGACCCGAGA ENSP00000417554.2:p.Val1830=
ENST00000477152.6:c.5418_5429delinsGGTGACCCGAGA ENSP00000419988.2:p.Val1806=
ENST00000478531.6:c.2184_2195delinsGGTGACCCGAGA ENSP00000420412.2:p.Val728=
ENST00000489037.2:c.5418_5429delinsGGTGACCCGAGA ENSP00000420781.2:p.Val1806=
ENST00000493919.6:c.2046_2057delinsGGTGACCCGAGA ENSP00000418819.2:p.Val682=
ENST00000494123.6:c.5496_5507delinsGGTGACCCGAGA ENSP00000419103.2:p.Val1832=
ENST00000497488.2:c.4608_4619delinsGGTGACCCGAGA ENSP00000418986.2:p.Val1536=
ENST00000618469.2:c.5496_5507delinsGGTGACCCGAGA ENSP00000478114.2:p.Val1832=
ENST00000634433.2:c.5373_5384delinsGGTGACCCGAGA ENSP00000489431.2:p.Val1791=
ENST00000644379.2:c.5562_5573delinsGGTGACCCGAGA ENSP00000496570.2:p.Val1854=
ENST00000644555.2:c.2046_2057delinsGGTGACCCGAGA ENSP00000494614.2:p.Val682=
ENST00000652672.2:c.5355_5366delinsGGTGACCCGAGA ENSP00000498906.2:p.Val1785=
ENST00000484087.6:c.2058_2069delinsGGTGACCCGAGA ENSP00000419481.2:p.Val686=
ENST00000700081.1:n.1379_1390delinsGGTGACCCGAGA
ENST00000700082.1:n.860_871delinsGGTGACCCGAGA
ENST00000357654.9:c.5496_5507delinsGGTGACCCGAGA MANE Select ENSP00000350283.3:p.Val1832=
ENST00000471181.7:c.5559_5570delinsGGTGACCCGAGA ENSP00000418960.2:p.Val1853=
ENST00000644379.1:c.1883_1894delinsGGTGACCCGAGA
ENST00000352993.7:c.2070_2081delinsGGTGACCCGAGA ENSP00000312236.5:p.Val690=
ENST00000357654.7:c.5496_5507delinsGGTGACCCGAGA ENSP00000350283.3:p.Val1832=
ENST00000461221.5:c.*5279_*5290delinsGGTGACCCGAGA ENSP00000418548.1:n.*5279_*5290delinsGGTGACCCGAGA
ENST00000468300.5:c.*10_*21delinsGGTGACCCGAGA ENSP00000417148.1:n.*10_*21delinsGGTGACCCGAGA
ENST00000471181.6:c.5559_5570delinsGGTGACCCGAGA ENSP00000418960.2:p.Val1853=
ENST00000491747.6:c.2184_2195delinsGGTGACCCGAGA ENSP00000420705.2:p.Val728=
ENST00000493795.5:c.5355_5366delinsGGTGACCCGAGA ENSP00000418775.1:p.Val1785=
ENST00000586385.5:c.426_437delinsGGTGACCCGAGA ENSP00000465818.1:p.Val142=
ENST00000591534.5:c.969_980delinsGGTGACCCGAGA ENSP00000467329.1:p.Val323=
ENST00000591849.5:c.195_206delinsGGTGACCCGAGA ENSP00000465347.1:p.Val65=
NM_007294.3:c.5496_5507delinsGGTGACCCGAGA , LRG_292t1:c.5496_5507delinsGGTGACCCGAGA NP_009225.1:p.Val1832=
NM_007297.3:c.5355_5366delinsGGTGACCCGAGA NP_009228.2:p.Val1785=
NM_007298.3:c.2184_2195delinsGGTGACCCGAGA NP_009229.2:p.Val728=
NM_007299.3:c.*10_*21delinsGGTGACCCGAGA NP_009230.2:n.*10_*21delinsGGTGACCCGAGA
NM_007300.3:c.5559_5570delinsGGTGACCCGAGA NP_009231.2:p.Val1853=
NR_027676.1:n.5632_5643delinsGGTGACCCGAGA
NM_007294.4:c.5496_5507delinsGGTGACCCGAGA MANE Select NP_009225.1:p.Val1832=
NM_007297.4:c.5355_5366delinsGGTGACCCGAGA NP_009228.2:p.Val1785=
NM_007299.4:c.*10_*21delinsGGTGACCCGAGA NP_009230.2:n.*10_*21delinsGGTGACCCGAGA
NM_007300.4:c.5559_5570delinsGGTGACCCGAGA NP_009231.2:p.Val1853=
NR_027676.2:n.5673_5684delinsGGTGACCCGAGA