Canonical Allele Identifier: CA2837995180

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43092391_43092392dup , CM000679.2:g.43092391_43092392dup	GRCh38
NC_000017.10:g.41244408_41244409dup , CM000679.1:g.41244408_41244409dup	GRCh37
NC_000017.9:g.38497934_38497935dup	NCBI36
NG_005905.2:g.125592_125593dup , LRG_292:g.125592_125593dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.3203_3204dup
ENST00000461574.2:c.3139_3140dup	ENSP00000417241.2:p.Gly1048Ter
ENST00000470026.6:c.3139_3140dup	ENSP00000419274.2:p.Gly1048Ter
ENST00000473961.6:c.3013_3014dup	ENSP00000420201.2:p.Gly1006Ter
ENST00000476777.6:c.3136_3137dup	ENSP00000417554.2:p.Gly1047Ter
ENST00000477152.6:c.3061_3062dup	ENSP00000419988.2:p.Gly1022Ter
ENST00000478531.6:c.785-1360_785-1359dup	ENSP00000420412.2:n.785-1360_785-1359dup
ENST00000489037.2:c.3061_3062dup	ENSP00000420781.2:p.Gly1022Ter
ENST00000493919.6:c.647-1360_647-1359dup	ENSP00000418819.2:n.647-1360_647-1359dup
ENST00000494123.6:c.3139_3140dup	ENSP00000419103.2:p.Gly1048Ter
ENST00000497488.2:c.2251_2252dup	ENSP00000418986.2:p.Gly752Ter
ENST00000618469.2:c.3139_3140dup	ENSP00000478114.2:p.Gly1048Ter
ENST00000634433.2:c.3016_3017dup	ENSP00000489431.2:p.Gly1007Ter
ENST00000644379.2:c.3139_3140dup	ENSP00000496570.2:p.Gly1048Ter
ENST00000644555.2:c.647-1360_647-1359dup	ENSP00000494614.2:n.647-1360_647-1359dup
ENST00000652672.2:c.2998_2999dup	ENSP00000498906.2:p.Gly1001Ter
ENST00000484087.6:c.665-1360_665-1359dup	ENSP00000419481.2:n.665-1360_665-1359dup
ENST00000700182.1:c.707-1360_707-1359dup	ENSP00000514849.1:n.707-1360_707-1359dup
ENST00000357654.9:c.3139_3140dup MANE Select	ENSP00000350283.3:p.Gly1048Ter
ENST00000471181.7:c.3139_3140dup	ENSP00000418960.2:p.Gly1048Ter
ENST00000352993.7:c.671-1360_671-1359dup	ENSP00000312236.5:n.671-1360_671-1359dup
ENST00000354071.7:c.3139_3140dup	ENSP00000326002.7:p.Gly1048Ter
ENST00000357654.7:c.3139_3140dup	ENSP00000350283.3:p.Gly1048Ter
ENST00000461221.5:c.*2922_*2923dup	ENSP00000418548.1:n.*2922_*2923dup
ENST00000468300.5:c.788-1360_788-1359dup	ENSP00000417148.1:n.788-1360_788-1359dup
ENST00000471181.6:c.3139_3140dup	ENSP00000418960.2:p.Gly1048Ter
ENST00000478531.5:c.785-1360_785-1359dup	ENSP00000420412.1:n.785-1360_785-1359dup
ENST00000484087.5:c.410-1360_410-1359dup	ENSP00000419481.1:n.410-1360_410-1359dup
ENST00000487825.5:c.413-1360_413-1359dup	ENSP00000418212.1:n.413-1360_413-1359dup
ENST00000491747.6:c.788-1360_788-1359dup	ENSP00000420705.2:n.788-1360_788-1359dup
ENST00000493795.5:c.2998_2999dup	ENSP00000418775.1:p.Gly1001Ter
ENST00000493919.5:c.647-1360_647-1359dup	ENSP00000418819.1:n.647-1360_647-1359dup
ENST00000586385.5:c.5-28441_5-28440dup	ENSP00000465818.1:n.5-28441_5-28440dup
ENST00000591534.5:c.-43-17871_-43-17870dup	ENSP00000467329.1:n.-43-17871_-43-17870dup
ENST00000591849.5:c.-99+32879_-99+32880dup	ENSP00000465347.1:n.-99+32879_-99+32880dup
NM_007294.3:c.3139_3140dup , LRG_292t1:c.3139_3140dup	NP_009225.1:p.Gly1048Ter
NM_007297.3:c.2998_2999dup	NP_009228.2:p.Gly1001Ter
NM_007298.3:c.788-1360_788-1359dup	NP_009229.2:n.788-1360_788-1359dup
NM_007299.3:c.788-1360_788-1359dup	NP_009230.2:n.788-1360_788-1359dup
NM_007300.3:c.3139_3140dup	NP_009231.2:p.Gly1048Ter
NR_027676.1:n.3275_3276dup
NM_007294.4:c.3139_3140dup MANE Select	NP_009225.1:p.Gly1048Ter
NM_007297.4:c.2998_2999dup	NP_009228.2:p.Gly1001Ter
NM_007299.4:c.788-1360_788-1359dup	NP_009230.2:n.788-1360_788-1359dup
NM_007300.4:c.3139_3140dup	NP_009231.2:p.Gly1048Ter
NR_027676.2:n.3316_3317dup