Canonical Allele Identifier: CA2260784901

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43094407_43094408delinsAG , CM000679.2:g.43094407_43094408delinsAG	GRCh38
NC_000017.10:g.41246424_41246425delinsAG , CM000679.1:g.41246424_41246425delinsAG	GRCh37
NC_000017.9:g.38499950_38499951delinsAG	NCBI36
NG_005905.2:g.123576_123577delinsCT , LRG_292:g.123576_123577delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.1187_1188delinsCT
ENST00000461574.2:c.1123_1124delinsCT	ENSP00000417241.2:p.Leu375=
ENST00000470026.6:c.1123_1124delinsCT	ENSP00000419274.2:p.Leu375=
ENST00000473961.6:c.997_998delinsCT	ENSP00000420201.2:p.Leu333=
ENST00000476777.6:c.1120_1121delinsCT	ENSP00000417554.2:p.Leu374=
ENST00000477152.6:c.1045_1046delinsCT	ENSP00000419988.2:p.Leu349=
ENST00000478531.6:c.784+336_784+337delinsCT	ENSP00000420412.2:n.784+336_784+337delinsCT
ENST00000489037.2:c.1045_1046delinsCT	ENSP00000420781.2:p.Leu349=
ENST00000493919.6:c.646+336_646+337delinsCT	ENSP00000418819.2:n.646+336_646+337delinsCT
ENST00000494123.6:c.1123_1124delinsCT	ENSP00000419103.2:p.Leu375=
ENST00000497488.2:c.235_236delinsCT	ENSP00000418986.2:p.Leu79=
ENST00000618469.2:c.1123_1124delinsCT	ENSP00000478114.2:p.Leu375=
ENST00000634433.2:c.1000_1001delinsCT	ENSP00000489431.2:p.Leu334=
ENST00000644379.2:c.1123_1124delinsCT	ENSP00000496570.2:p.Leu375=
ENST00000644555.2:c.646+336_646+337delinsCT	ENSP00000494614.2:n.646+336_646+337delinsCT
ENST00000652672.2:c.982_983delinsCT	ENSP00000498906.2:p.Leu328=
ENST00000484087.6:c.664+336_664+337delinsCT	ENSP00000419481.2:n.664+336_664+337delinsCT
ENST00000700182.1:c.706+336_706+337delinsCT	ENSP00000514849.1:n.706+336_706+337delinsCT
ENST00000700183.1:c.*1131_*1132delinsCT	ENSP00000514850.1:n.*1131_*1132delinsCT
ENST00000357654.9:c.1123_1124delinsCT MANE Select	ENSP00000350283.3:p.Leu375=
ENST00000471181.7:c.1123_1124delinsCT	ENSP00000418960.2:p.Leu375=
ENST00000652672.1:c.982_983delinsCT	ENSP00000498906.1:p.Leu328=
ENST00000352993.7:c.670+1438_670+1439delinsCT	ENSP00000312236.5:n.670+1438_670+1439delinsCT
ENST00000354071.7:c.1123_1124delinsCT	ENSP00000326002.7:p.Leu375=
ENST00000357654.7:c.1123_1124delinsCT	ENSP00000350283.3:p.Leu375=
ENST00000412061.3:c.474_475delinsCT
ENST00000461221.5:c.*906_*907delinsCT	ENSP00000418548.1:n.*906_*907delinsCT
ENST00000468300.5:c.787+336_787+337delinsCT	ENSP00000417148.1:n.787+336_787+337delinsCT
ENST00000470026.5:c.1123_1124delinsCT	ENSP00000419274.1:p.Leu375=
ENST00000471181.6:c.1123_1124delinsCT	ENSP00000418960.2:p.Leu375=
ENST00000473961.5:c.720_721delinsCT
ENST00000477152.5:c.1045_1046delinsCT	ENSP00000419988.1:p.Leu349=
ENST00000478531.5:c.784+336_784+337delinsCT	ENSP00000420412.1:n.784+336_784+337delinsCT
ENST00000484087.5:c.409+336_409+337delinsCT	ENSP00000419481.1:n.409+336_409+337delinsCT
ENST00000487825.5:c.412+336_412+337delinsCT	ENSP00000418212.1:n.412+336_412+337delinsCT
ENST00000491747.6:c.787+336_787+337delinsCT	ENSP00000420705.2:n.787+336_787+337delinsCT
ENST00000492859.5:c.*1059_*1060delinsCT	ENSP00000420253.1:n.*1059_*1060delinsCT
ENST00000493795.5:c.982_983delinsCT	ENSP00000418775.1:p.Leu328=
ENST00000493919.5:c.646+336_646+337delinsCT	ENSP00000418819.1:n.646+336_646+337delinsCT
ENST00000494123.5:c.1123_1124delinsCT	ENSP00000419103.1:p.Leu375=
ENST00000497488.1:c.235_236delinsCT	ENSP00000418986.1:p.Leu79=
ENST00000586385.5:c.5-30457_5-30456delinsCT	ENSP00000465818.1:n.5-30457_5-30456delinsCT
ENST00000591534.5:c.-43-19887_-43-19886delinsCT	ENSP00000467329.1:n.-43-19887_-43-19886delinsCT
ENST00000591849.5:c.-99+30863_-99+30864delinsCT	ENSP00000465347.1:n.-99+30863_-99+30864delinsCT
ENST00000634433.1:c.1000_1001delinsCT	ENSP00000489431.1:p.Leu334=
NM_007294.3:c.1123_1124delinsCT , LRG_292t1:c.1123_1124delinsCT	NP_009225.1:p.Leu375=
NM_007297.3:c.982_983delinsCT	NP_009228.2:p.Leu328=
NM_007298.3:c.787+336_787+337delinsCT	NP_009229.2:n.787+336_787+337delinsCT
NM_007299.3:c.787+336_787+337delinsCT	NP_009230.2:n.787+336_787+337delinsCT
NM_007300.3:c.1123_1124delinsCT	NP_009231.2:p.Leu375=
NR_027676.1:n.1259_1260delinsCT
NM_007294.4:c.1123_1124delinsCT MANE Select	NP_009225.1:p.Leu375=
NM_007297.4:c.982_983delinsCT	NP_009228.2:p.Leu328=
NM_007299.4:c.787+336_787+337delinsCT	NP_009230.2:n.787+336_787+337delinsCT
NM_007300.4:c.1123_1124delinsCT	NP_009231.2:p.Leu375=
NR_027676.2:n.1300_1301delinsCT