Canonical Allele Identifier: CA2260784605

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43094093_43094103delinsTTTCAGTTACA , CM000679.2:g.43094093_43094103delinsTTTCAGTTACA	GRCh38
NC_000017.10:g.41246110_41246120delinsTTTCAGTTACA , CM000679.1:g.41246110_41246120delinsTTTCAGTTACA	GRCh37
NC_000017.9:g.38499636_38499646delinsTTTCAGTTACA	NCBI36
NG_005905.2:g.123881_123891delinsTGTAACTGAAA , LRG_292:g.123881_123891delinsTGTAACTGAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.1492_1502delinsTGTAACTGAAA
ENST00000461574.2:c.1428_1438delinsTGTAACTGAAA	ENSP00000417241.2:p.His476=
ENST00000470026.6:c.1428_1438delinsTGTAACTGAAA	ENSP00000419274.2:p.His476=
ENST00000473961.6:c.1302_1312delinsTGTAACTGAAA	ENSP00000420201.2:p.His434=
ENST00000476777.6:c.1425_1435delinsTGTAACTGAAA	ENSP00000417554.2:p.His475=
ENST00000477152.6:c.1350_1360delinsTGTAACTGAAA	ENSP00000419988.2:p.His450=
ENST00000478531.6:c.784+641_784+651delinsTGTAACTGAAA	ENSP00000420412.2:n.784+641_784+651delinsTGTAACTGAAA
ENST00000489037.2:c.1350_1360delinsTGTAACTGAAA	ENSP00000420781.2:p.His450=
ENST00000493919.6:c.646+641_646+651delinsTGTAACTGAAA	ENSP00000418819.2:n.646+641_646+651delinsTGTAACTGAAA
ENST00000494123.6:c.1428_1438delinsTGTAACTGAAA	ENSP00000419103.2:p.His476=
ENST00000497488.2:c.540_550delinsTGTAACTGAAA	ENSP00000418986.2:p.His180=
ENST00000618469.2:c.1428_1438delinsTGTAACTGAAA	ENSP00000478114.2:p.His476=
ENST00000634433.2:c.1305_1315delinsTGTAACTGAAA	ENSP00000489431.2:p.His435=
ENST00000644379.2:c.1428_1438delinsTGTAACTGAAA	ENSP00000496570.2:p.His476=
ENST00000644555.2:c.646+641_646+651delinsTGTAACTGAAA	ENSP00000494614.2:n.646+641_646+651delinsTGTAACTGAAA
ENST00000652672.2:c.1287_1297delinsTGTAACTGAAA	ENSP00000498906.2:p.His429=
ENST00000484087.6:c.664+641_664+651delinsTGTAACTGAAA	ENSP00000419481.2:n.664+641_664+651delinsTGTAACTGAAA
ENST00000700182.1:c.706+641_706+651delinsTGTAACTGAAA	ENSP00000514849.1:n.706+641_706+651delinsTGTAACTGAAA
ENST00000700183.1:c.*1436_*1446delinsTGTAACTGAAA	ENSP00000514850.1:n.*1436_*1446delinsTGTAACTGAAA
ENST00000357654.9:c.1428_1438delinsTGTAACTGAAA MANE Select	ENSP00000350283.3:p.His476=
ENST00000471181.7:c.1428_1438delinsTGTAACTGAAA	ENSP00000418960.2:p.His476=
ENST00000652672.1:c.1287_1297delinsTGTAACTGAAA	ENSP00000498906.1:p.His429=
ENST00000352993.7:c.670+1743_670+1753delinsTGTAACTGAAA	ENSP00000312236.5:n.670+1743_670+1753delinsTGTAACTGAAA
ENST00000354071.7:c.1428_1438delinsTGTAACTGAAA	ENSP00000326002.7:p.His476=
ENST00000357654.7:c.1428_1438delinsTGTAACTGAAA	ENSP00000350283.3:p.His476=
ENST00000412061.3:c.779_789delinsTGTAACTGAAA
ENST00000461221.5:c.*1211_*1221delinsTGTAACTGAAA	ENSP00000418548.1:n.*1211_*1221delinsTGTAACTGAAA
ENST00000468300.5:c.787+641_787+651delinsTGTAACTGAAA	ENSP00000417148.1:n.787+641_787+651delinsTGTAACTGAAA
ENST00000470026.5:c.1428_1438delinsTGTAACTGAAA	ENSP00000419274.1:p.His476=
ENST00000471181.6:c.1428_1438delinsTGTAACTGAAA	ENSP00000418960.2:p.His476=
ENST00000477152.5:c.1350_1360delinsTGTAACTGAAA	ENSP00000419988.1:p.His450=
ENST00000478531.5:c.784+641_784+651delinsTGTAACTGAAA	ENSP00000420412.1:n.784+641_784+651delinsTGTAACTGAAA
ENST00000484087.5:c.409+641_409+651delinsTGTAACTGAAA	ENSP00000419481.1:n.409+641_409+651delinsTGTAACTGAAA
ENST00000487825.5:c.412+641_412+651delinsTGTAACTGAAA	ENSP00000418212.1:n.412+641_412+651delinsTGTAACTGAAA
ENST00000491747.6:c.787+641_787+651delinsTGTAACTGAAA	ENSP00000420705.2:n.787+641_787+651delinsTGTAACTGAAA
ENST00000493795.5:c.1287_1297delinsTGTAACTGAAA	ENSP00000418775.1:p.His429=
ENST00000493919.5:c.646+641_646+651delinsTGTAACTGAAA	ENSP00000418819.1:n.646+641_646+651delinsTGTAACTGAAA
ENST00000586385.5:c.5-30152_5-30142delinsTGTAACTGAAA	ENSP00000465818.1:n.5-30152_5-30142delinsTGTAACTGAAA
ENST00000591534.5:c.-43-19582_-43-19572delinsTGTAACTGAAA	ENSP00000467329.1:n.-43-19582_-43-19572delinsTGTAACTGAAA
ENST00000591849.5:c.-99+31168_-99+31178delinsTGTAACTGAAA	ENSP00000465347.1:n.-99+31168_-99+31178delinsTGTAACTGAAA
ENST00000634433.1:c.1305_1315delinsTGTAACTGAAA	ENSP00000489431.1:p.His435=
NM_007294.3:c.1428_1438delinsTGTAACTGAAA , LRG_292t1:c.1428_1438delinsTGTAACTGAAA	NP_009225.1:p.His476=
NM_007297.3:c.1287_1297delinsTGTAACTGAAA	NP_009228.2:p.His429=
NM_007298.3:c.787+641_787+651delinsTGTAACTGAAA	NP_009229.2:n.787+641_787+651delinsTGTAACTGAAA
NM_007299.3:c.787+641_787+651delinsTGTAACTGAAA	NP_009230.2:n.787+641_787+651delinsTGTAACTGAAA
NM_007300.3:c.1428_1438delinsTGTAACTGAAA	NP_009231.2:p.His476=
NR_027676.1:n.1564_1574delinsTGTAACTGAAA
NM_007294.4:c.1428_1438delinsTGTAACTGAAA MANE Select	NP_009225.1:p.His476=
NM_007297.4:c.1287_1297delinsTGTAACTGAAA	NP_009228.2:p.His429=
NM_007299.4:c.787+641_787+651delinsTGTAACTGAAA	NP_009230.2:n.787+641_787+651delinsTGTAACTGAAA
NM_007300.4:c.1428_1438delinsTGTAACTGAAA	NP_009231.2:p.His476=
NR_027676.2:n.1605_1615delinsTGTAACTGAAA