Canonical Allele Identifier: CA2260784977

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43094490_43094491delinsCA , CM000679.2:g.43094490_43094491delinsCA	GRCh38
NC_000017.10:g.41246507_41246508delinsCA , CM000679.1:g.41246507_41246508delinsCA	GRCh37
NC_000017.9:g.38500033_38500034delinsCA	NCBI36
NG_005905.2:g.123493_123494delinsTG , LRG_292:g.123493_123494delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.1104_1105delinsTG
ENST00000461574.2:c.1040_1041delinsTG	ENSP00000417241.2:p.Leu347=
ENST00000470026.6:c.1040_1041delinsTG	ENSP00000419274.2:p.Leu347=
ENST00000473961.6:c.914_915delinsTG	ENSP00000420201.2:p.Leu305=
ENST00000476777.6:c.1037_1038delinsTG	ENSP00000417554.2:p.Leu346=
ENST00000477152.6:c.962_963delinsTG	ENSP00000419988.2:p.Leu321=
ENST00000478531.6:c.784+253_784+254delinsTG	ENSP00000420412.2:n.784+253_784+254delinsTG
ENST00000489037.2:c.962_963delinsTG	ENSP00000420781.2:p.Leu321=
ENST00000493919.6:c.646+253_646+254delinsTG	ENSP00000418819.2:n.646+253_646+254delinsTG
ENST00000494123.6:c.1040_1041delinsTG	ENSP00000419103.2:p.Leu347=
ENST00000497488.2:c.152_153delinsTG	ENSP00000418986.2:p.Leu51=
ENST00000618469.2:c.1040_1041delinsTG	ENSP00000478114.2:p.Leu347=
ENST00000634433.2:c.917_918delinsTG	ENSP00000489431.2:p.Leu306=
ENST00000644379.2:c.1040_1041delinsTG	ENSP00000496570.2:p.Leu347=
ENST00000644555.2:c.646+253_646+254delinsTG	ENSP00000494614.2:n.646+253_646+254delinsTG
ENST00000652672.2:c.899_900delinsTG	ENSP00000498906.2:p.Leu300=
ENST00000484087.6:c.664+253_664+254delinsTG	ENSP00000419481.2:n.664+253_664+254delinsTG
ENST00000700182.1:c.706+253_706+254delinsTG	ENSP00000514849.1:n.706+253_706+254delinsTG
ENST00000700183.1:c.*1048_*1049delinsTG	ENSP00000514850.1:n.*1048_*1049delinsTG
ENST00000357654.9:c.1040_1041delinsTG MANE Select	ENSP00000350283.3:p.Leu347=
ENST00000471181.7:c.1040_1041delinsTG	ENSP00000418960.2:p.Leu347=
ENST00000642945.1:c.*914_*915delinsTG	ENSP00000495897.1:n.*914_*915delinsTG
ENST00000652672.1:c.899_900delinsTG	ENSP00000498906.1:p.Leu300=
ENST00000352993.7:c.670+1355_670+1356delinsTG	ENSP00000312236.5:n.670+1355_670+1356delinsTG
ENST00000354071.7:c.1040_1041delinsTG	ENSP00000326002.7:p.Leu347=
ENST00000357654.7:c.1040_1041delinsTG	ENSP00000350283.3:p.Leu347=
ENST00000412061.3:c.391_392delinsTG
ENST00000461221.5:c.*823_*824delinsTG	ENSP00000418548.1:n.*823_*824delinsTG
ENST00000468300.5:c.787+253_787+254delinsTG	ENSP00000417148.1:n.787+253_787+254delinsTG
ENST00000470026.5:c.1040_1041delinsTG	ENSP00000419274.1:p.Leu347=
ENST00000471181.6:c.1040_1041delinsTG	ENSP00000418960.2:p.Leu347=
ENST00000473961.5:c.637_638delinsTG
ENST00000477152.5:c.962_963delinsTG	ENSP00000419988.1:p.Leu321=
ENST00000478531.5:c.784+253_784+254delinsTG	ENSP00000420412.1:n.784+253_784+254delinsTG
ENST00000484087.5:c.409+253_409+254delinsTG	ENSP00000419481.1:n.409+253_409+254delinsTG
ENST00000487825.5:c.412+253_412+254delinsTG	ENSP00000418212.1:n.412+253_412+254delinsTG
ENST00000491747.6:c.787+253_787+254delinsTG	ENSP00000420705.2:n.787+253_787+254delinsTG
ENST00000492859.5:c.*976_*977delinsTG	ENSP00000420253.1:n.*976_*977delinsTG
ENST00000493795.5:c.899_900delinsTG	ENSP00000418775.1:p.Leu300=
ENST00000493919.5:c.646+253_646+254delinsTG	ENSP00000418819.1:n.646+253_646+254delinsTG
ENST00000494123.5:c.1040_1041delinsTG	ENSP00000419103.1:p.Leu347=
ENST00000497488.1:c.152_153delinsTG	ENSP00000418986.1:p.Leu51=
ENST00000586385.5:c.5-30540_5-30539delinsTG	ENSP00000465818.1:n.5-30540_5-30539delinsTG
ENST00000591534.5:c.-43-19970_-43-19969delinsTG	ENSP00000467329.1:n.-43-19970_-43-19969delinsTG
ENST00000591849.5:c.-99+30780_-99+30781delinsTG	ENSP00000465347.1:n.-99+30780_-99+30781delinsTG
ENST00000634433.1:c.917_918delinsTG	ENSP00000489431.1:p.Leu306=
NM_007294.3:c.1040_1041delinsTG , LRG_292t1:c.1040_1041delinsTG	NP_009225.1:p.Leu347=
NM_007297.3:c.899_900delinsTG	NP_009228.2:p.Leu300=
NM_007298.3:c.787+253_787+254delinsTG	NP_009229.2:n.787+253_787+254delinsTG
NM_007299.3:c.787+253_787+254delinsTG	NP_009230.2:n.787+253_787+254delinsTG
NM_007300.3:c.1040_1041delinsTG	NP_009231.2:p.Leu347=
NR_027676.1:n.1176_1177delinsTG
NM_007294.4:c.1040_1041delinsTG MANE Select	NP_009225.1:p.Leu347=
NM_007297.4:c.899_900delinsTG	NP_009228.2:p.Leu300=
NM_007299.4:c.787+253_787+254delinsTG	NP_009230.2:n.787+253_787+254delinsTG
NM_007300.4:c.1040_1041delinsTG	NP_009231.2:p.Leu347=
NR_027676.2:n.1217_1218delinsTG