Canonical Allele Identifier: CA2260782947

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43092447_43092448delinsAC , CM000679.2:g.43092447_43092448delinsAC	GRCh38
NC_000017.10:g.41244464_41244465delinsAC , CM000679.1:g.41244464_41244465delinsAC	GRCh37
NC_000017.9:g.38497990_38497991delinsAC	NCBI36
NG_005905.2:g.125536_125537delinsGT , LRG_292:g.125536_125537delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.3147_3148delinsGT
ENST00000461574.2:c.3083_3084delinsGT	ENSP00000417241.2:p.Arg1028=
ENST00000470026.6:c.3083_3084delinsGT	ENSP00000419274.2:p.Arg1028=
ENST00000473961.6:c.2957_2958delinsGT	ENSP00000420201.2:p.Arg986=
ENST00000476777.6:c.3080_3081delinsGT	ENSP00000417554.2:p.Arg1027=
ENST00000477152.6:c.3005_3006delinsGT	ENSP00000419988.2:p.Arg1002=
ENST00000478531.6:c.785-1416_785-1415delinsGT	ENSP00000420412.2:n.785-1416_785-1415delinsGT
ENST00000489037.2:c.3005_3006delinsGT	ENSP00000420781.2:p.Arg1002=
ENST00000493919.6:c.647-1416_647-1415delinsGT	ENSP00000418819.2:n.647-1416_647-1415delinsGT
ENST00000494123.6:c.3083_3084delinsGT	ENSP00000419103.2:p.Arg1028=
ENST00000497488.2:c.2195_2196delinsGT	ENSP00000418986.2:p.Arg732=
ENST00000618469.2:c.3083_3084delinsGT	ENSP00000478114.2:p.Arg1028=
ENST00000634433.2:c.2960_2961delinsGT	ENSP00000489431.2:p.Arg987=
ENST00000644379.2:c.3083_3084delinsGT	ENSP00000496570.2:p.Arg1028=
ENST00000644555.2:c.647-1416_647-1415delinsGT	ENSP00000494614.2:n.647-1416_647-1415delinsGT
ENST00000652672.2:c.2942_2943delinsGT	ENSP00000498906.2:p.Arg981=
ENST00000484087.6:c.665-1416_665-1415delinsGT	ENSP00000419481.2:n.665-1416_665-1415delinsGT
ENST00000700182.1:c.707-1416_707-1415delinsGT	ENSP00000514849.1:n.707-1416_707-1415delinsGT
ENST00000357654.9:c.3083_3084delinsGT MANE Select	ENSP00000350283.3:p.Arg1028=
ENST00000471181.7:c.3083_3084delinsGT	ENSP00000418960.2:p.Arg1028=
ENST00000352993.7:c.671-1416_671-1415delinsGT	ENSP00000312236.5:n.671-1416_671-1415delinsGT
ENST00000354071.7:c.3083_3084delinsGT	ENSP00000326002.7:p.Arg1028=
ENST00000357654.7:c.3083_3084delinsGT	ENSP00000350283.3:p.Arg1028=
ENST00000461221.5:c.*2866_*2867delinsGT	ENSP00000418548.1:n.*2866_*2867delinsGT
ENST00000468300.5:c.788-1416_788-1415delinsGT	ENSP00000417148.1:n.788-1416_788-1415delinsGT
ENST00000471181.6:c.3083_3084delinsGT	ENSP00000418960.2:p.Arg1028=
ENST00000478531.5:c.785-1416_785-1415delinsGT	ENSP00000420412.1:n.785-1416_785-1415delinsGT
ENST00000484087.5:c.410-1416_410-1415delinsGT	ENSP00000419481.1:n.410-1416_410-1415delinsGT
ENST00000487825.5:c.413-1416_413-1415delinsGT	ENSP00000418212.1:n.413-1416_413-1415delinsGT
ENST00000491747.6:c.788-1416_788-1415delinsGT	ENSP00000420705.2:n.788-1416_788-1415delinsGT
ENST00000493795.5:c.2942_2943delinsGT	ENSP00000418775.1:p.Arg981=
ENST00000493919.5:c.647-1416_647-1415delinsGT	ENSP00000418819.1:n.647-1416_647-1415delinsGT
ENST00000586385.5:c.5-28497_5-28496delinsGT	ENSP00000465818.1:n.5-28497_5-28496delinsGT
ENST00000591534.5:c.-43-17927_-43-17926delinsGT	ENSP00000467329.1:n.-43-17927_-43-17926delinsGT
ENST00000591849.5:c.-99+32823_-99+32824delinsGT	ENSP00000465347.1:n.-99+32823_-99+32824delinsGT
NM_007294.3:c.3083_3084delinsGT , LRG_292t1:c.3083_3084delinsGT	NP_009225.1:p.Arg1028=
NM_007297.3:c.2942_2943delinsGT	NP_009228.2:p.Arg981=
NM_007298.3:c.788-1416_788-1415delinsGT	NP_009229.2:n.788-1416_788-1415delinsGT
NM_007299.3:c.788-1416_788-1415delinsGT	NP_009230.2:n.788-1416_788-1415delinsGT
NM_007300.3:c.3083_3084delinsGT	NP_009231.2:p.Arg1028=
NR_027676.1:n.3219_3220delinsGT
NM_007294.4:c.3083_3084delinsGT MANE Select	NP_009225.1:p.Arg1028=
NM_007297.4:c.2942_2943delinsGT	NP_009228.2:p.Arg981=
NM_007299.4:c.788-1416_788-1415delinsGT	NP_009230.2:n.788-1416_788-1415delinsGT
NM_007300.4:c.3083_3084delinsGT	NP_009231.2:p.Arg1028=
NR_027676.2:n.3260_3261delinsGT