Canonical Allele Identifier: CA2739265616

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 2824395
• ClinVar RCV Id: RCV003645689

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43091750_43091758dup , CM000679.2:g.43091750_43091758dup	GRCh38
NC_000017.10:g.41243767_41243775dup , CM000679.1:g.41243767_41243775dup	GRCh37
NC_000017.9:g.38497293_38497301dup	NCBI36
NG_005905.2:g.126226_126234dup , LRG_292:g.126226_126234dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000354071.8:n.3837_3845dup
ENST00000461574.2:c.3773_3781dup	ENSP00000417241.2:p.Leu1261Ter
ENST00000470026.6:c.3773_3781dup	ENSP00000419274.2:p.Leu1261Ter
ENST00000473961.6:c.3647_3655dup	ENSP00000420201.2:p.Leu1219Ter
ENST00000476777.6:c.3770_3778dup	ENSP00000417554.2:p.Leu1260Ter
ENST00000477152.6:c.3695_3703dup	ENSP00000419988.2:p.Leu1235Ter
ENST00000478531.6:c.785-726_785-718dup	ENSP00000420412.2:n.785-726_785-718dup
ENST00000489037.2:c.3695_3703dup	ENSP00000420781.2:p.Leu1235Ter
ENST00000493919.6:c.647-726_647-718dup	ENSP00000418819.2:n.647-726_647-718dup
ENST00000494123.6:c.3773_3781dup	ENSP00000419103.2:p.Leu1261Ter
ENST00000497488.2:c.2885_2893dup	ENSP00000418986.2:p.Leu965Ter
ENST00000618469.2:c.3773_3781dup	ENSP00000478114.2:p.Leu1261Ter
ENST00000634433.2:c.3650_3658dup	ENSP00000489431.2:p.Leu1220Ter
ENST00000644379.2:c.3773_3781dup	ENSP00000496570.2:p.Leu1261Ter
ENST00000644555.2:c.647-726_647-718dup	ENSP00000494614.2:n.647-726_647-718dup
ENST00000652672.2:c.3632_3640dup	ENSP00000498906.2:p.Leu1214Ter
ENST00000484087.6:c.665-726_665-718dup	ENSP00000419481.2:n.665-726_665-718dup
ENST00000700182.1:c.707-726_707-718dup	ENSP00000514849.1:n.707-726_707-718dup
ENST00000357654.9:c.3773_3781dup MANE Select	ENSP00000350283.3:p.Leu1261Ter
ENST00000471181.7:c.3773_3781dup	ENSP00000418960.2:p.Leu1261Ter
ENST00000644379.1:c.94_102dup
ENST00000352993.7:c.671-726_671-718dup	ENSP00000312236.5:n.671-726_671-718dup
ENST00000354071.7:c.3773_3781dup	ENSP00000326002.7:p.Leu1261Ter
ENST00000357654.7:c.3773_3781dup	ENSP00000350283.3:p.Leu1261Ter
ENST00000461221.5:c.*3556_*3564dup	ENSP00000418548.1:n.*3556_*3564dup
ENST00000461574.1:c.67_75dup
ENST00000468300.5:c.788-726_788-718dup	ENSP00000417148.1:n.788-726_788-718dup
ENST00000471181.6:c.3773_3781dup	ENSP00000418960.2:p.Leu1261Ter
ENST00000478531.5:c.785-726_785-718dup	ENSP00000420412.1:n.785-726_785-718dup
ENST00000484087.5:c.410-726_410-718dup	ENSP00000419481.1:n.410-726_410-718dup
ENST00000487825.5:c.413-726_413-718dup	ENSP00000418212.1:n.413-726_413-718dup
ENST00000491747.6:c.788-726_788-718dup	ENSP00000420705.2:n.788-726_788-718dup
ENST00000493795.5:c.3632_3640dup	ENSP00000418775.1:p.Leu1214Ter
ENST00000493919.5:c.647-726_647-718dup	ENSP00000418819.1:n.647-726_647-718dup
ENST00000586385.5:c.5-27807_5-27799dup	ENSP00000465818.1:n.5-27807_5-27799dup
ENST00000591534.5:c.-43-17237_-43-17229dup	ENSP00000467329.1:n.-43-17237_-43-17229du...
ENST00000591849.5:c.-99+33513_-99+33521dup	ENSP00000465347.1:n.-99+33513_-99+33521du...
NM_007294.3:c.3773_3781dup , LRG_292t1:c.3773_3781dup	NP_009225.1:p.Leu1261Ter
NM_007297.3:c.3632_3640dup	NP_009228.2:p.Leu1214Ter
NM_007298.3:c.788-726_788-718dup	NP_009229.2:n.788-726_788-718dup
NM_007299.3:c.788-726_788-718dup	NP_009230.2:n.788-726_788-718dup
NM_007300.3:c.3773_3781dup	NP_009231.2:p.Leu1261Ter
NR_027676.1:n.3909_3917dup
NM_007294.4:c.3773_3781dup MANE Select	NP_009225.1:p.Leu1261Ter
NM_007297.4:c.3632_3640dup	NP_009228.2:p.Leu1214Ter
NM_007299.4:c.788-726_788-718dup	NP_009230.2:n.788-726_788-718dup
NM_007300.4:c.3773_3781dup	NP_009231.2:p.Leu1261Ter
NR_027676.2:n.3950_3958dup