Canonical Allele Identifier: CA916084314

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43093651_43093654dup , CM000679.2:g.43093651_43093654dup	GRCh38
NC_000017.10:g.41245668_41245671dup , CM000679.1:g.41245668_41245671dup	GRCh37
NC_000017.9:g.38499194_38499197dup	NCBI36
NG_005905.2:g.124330_124333dup , LRG_292:g.124330_124333dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000354071.8:n.1941_1944dup
ENST00000461574.2:c.1877_1880dup	ENSP00000417241.2:p.Arg629GlnfsTer2
ENST00000470026.6:c.1877_1880dup	ENSP00000419274.2:p.Arg629GlnfsTer2
ENST00000473961.6:c.1751_1754dup	ENSP00000420201.2:p.Arg587GlnfsTer2
ENST00000476777.6:c.1874_1877dup	ENSP00000417554.2:p.Arg628GlnfsTer2
ENST00000477152.6:c.1799_1802dup	ENSP00000419988.2:p.Arg603GlnfsTer2
ENST00000478531.6:c.784+1090_784+1093dup	ENSP00000420412.2:n.784+1090_784+1093dup
ENST00000489037.2:c.1799_1802dup	ENSP00000420781.2:p.Arg603GlnfsTer2
ENST00000493919.6:c.646+1090_646+1093dup	ENSP00000418819.2:n.646+1090_646+1093dup
ENST00000494123.6:c.1877_1880dup	ENSP00000419103.2:p.Arg629GlnfsTer2
ENST00000497488.2:c.989_992dup	ENSP00000418986.2:p.Arg333GlnfsTer2
ENST00000618469.2:c.1877_1880dup	ENSP00000478114.2:p.Arg629GlnfsTer2
ENST00000634433.2:c.1754_1757dup	ENSP00000489431.2:p.Arg588GlnfsTer2
ENST00000644379.2:c.1877_1880dup	ENSP00000496570.2:p.Arg629GlnfsTer2
ENST00000644555.2:c.646+1090_646+1093dup	ENSP00000494614.2:n.646+1090_646+1093dup
ENST00000652672.2:c.1736_1739dup	ENSP00000498906.2:p.Arg582GlnfsTer2
ENST00000484087.6:c.664+1090_664+1093dup	ENSP00000419481.2:n.664+1090_664+1093dup
ENST00000700182.1:c.706+1090_706+1093dup	ENSP00000514849.1:n.706+1090_706+1093dup
ENST00000357654.9:c.1877_1880dup MANE Select	ENSP00000350283.3:p.Arg629GlnfsTer2
ENST00000471181.7:c.1877_1880dup	ENSP00000418960.2:p.Arg629GlnfsTer2
ENST00000652672.1:c.1736_1739dup	ENSP00000498906.1:p.Arg582GlnfsTer2
ENST00000352993.7:c.670+2192_670+2195dup	ENSP00000312236.5:n.670+2192_670+2195dup
ENST00000354071.7:c.1877_1880dup	ENSP00000326002.7:p.Arg629GlnfsTer2
ENST00000357654.7:c.1877_1880dup	ENSP00000350283.3:p.Arg629GlnfsTer2
ENST00000412061.3:c.1228_1231dup
ENST00000461221.5:c.*1660_*1663dup	ENSP00000418548.1:n.*1660_*1663dup
ENST00000468300.5:c.787+1090_787+1093dup	ENSP00000417148.1:n.787+1090_787+1093dup
ENST00000470026.5:c.1877_1880dup	ENSP00000419274.1:p.Arg629GlnfsTer2
ENST00000471181.6:c.1877_1880dup	ENSP00000418960.2:p.Arg629GlnfsTer2
ENST00000477152.5:c.1799_1802dup	ENSP00000419988.1:p.Arg603GlnfsTer2
ENST00000478531.5:c.784+1090_784+1093dup	ENSP00000420412.1:n.784+1090_784+1093dup
ENST00000484087.5:c.409+1090_409+1093dup	ENSP00000419481.1:n.409+1090_409+1093dup
ENST00000487825.5:c.412+1090_412+1093dup	ENSP00000418212.1:n.412+1090_412+1093dup
ENST00000491747.6:c.787+1090_787+1093dup	ENSP00000420705.2:n.787+1090_787+1093dup
ENST00000493795.5:c.1736_1739dup	ENSP00000418775.1:p.Arg582GlnfsTer2
ENST00000493919.5:c.646+1090_646+1093dup	ENSP00000418819.1:n.646+1090_646+1093dup
ENST00000586385.5:c.5-29703_5-29700dup	ENSP00000465818.1:n.5-29703_5-29700dup
ENST00000591534.5:c.-43-19133_-43-19130dup	ENSP00000467329.1:n.-43-19133_-43-19130du...
ENST00000591849.5:c.-99+31617_-99+31620dup	ENSP00000465347.1:n.-99+31617_-99+31620du...
ENST00000634433.1:c.1754_1757dup	ENSP00000489431.1:p.Arg588GlnfsTer2
NM_007294.3:c.1877_1880dup , LRG_292t1:c.1877_1880dup	NP_009225.1:p.Arg629GlnfsTer2
NM_007297.3:c.1736_1739dup	NP_009228.2:p.Arg582GlnfsTer2
NM_007298.3:c.787+1090_787+1093dup	NP_009229.2:n.787+1090_787+1093dup
NM_007299.3:c.787+1090_787+1093dup	NP_009230.2:n.787+1090_787+1093dup
NM_007300.3:c.1877_1880dup	NP_009231.2:p.Arg629GlnfsTer2
NR_027676.1:n.2013_2016dup
NM_007294.4:c.1877_1880dup MANE Select	NP_009225.1:p.Arg629GlnfsTer2
NM_007297.4:c.1736_1739dup	NP_009228.2:p.Arg582GlnfsTer2
NM_007299.4:c.787+1090_787+1093dup	NP_009230.2:n.787+1090_787+1093dup
NM_007300.4:c.1877_1880dup	NP_009231.2:p.Arg629GlnfsTer2
NR_027676.2:n.2054_2057dup