Canonical Allele Identifier: CA983884321

Gene: BRCA1

Linked Data

• dbSNP Id: rs2053466213
• gnomAD v3: 17-43091400-A-AGACTG
• gnomAD v4: 17-43091400-A-AGACTG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43091402_43091406dup , CM000679.2:g.43091402_43091406dup	GRCh38
NC_000017.10:g.41243419_41243423dup , CM000679.1:g.41243419_41243423dup	GRCh37
NC_000017.9:g.38496945_38496949dup	NCBI36
NG_005905.2:g.126579_126583dup , LRG_292:g.126579_126583dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.4190_4194dup
ENST00000461574.2:c.4096+30_4096+34dup	ENSP00000417241.2:n.4096+30_4096+34dup
ENST00000470026.6:c.4096+30_4096+34dup	ENSP00000419274.2:n.4096+30_4096+34dup
ENST00000473961.6:c.3970+30_3970+34dup	ENSP00000420201.2:n.3970+30_3970+34dup
ENST00000476777.6:c.4093+30_4093+34dup	ENSP00000417554.2:n.4093+30_4093+34dup
ENST00000477152.6:c.4018+30_4018+34dup	ENSP00000419988.2:n.4018+30_4018+34dup
ENST00000478531.6:c.785-373_785-369dup	ENSP00000420412.2:n.785-373_785-369dup
ENST00000489037.2:c.4018+30_4018+34dup	ENSP00000420781.2:n.4018+30_4018+34dup
ENST00000493919.6:c.647-373_647-369dup	ENSP00000418819.2:n.647-373_647-369dup
ENST00000494123.6:c.4096+30_4096+34dup	ENSP00000419103.2:n.4096+30_4096+34dup
ENST00000497488.2:c.3208+30_3208+34dup	ENSP00000418986.2:n.3208+30_3208+34dup
ENST00000618469.2:c.4096+30_4096+34dup	ENSP00000478114.2:n.4096+30_4096+34dup
ENST00000634433.2:c.3973+30_3973+34dup	ENSP00000489431.2:n.3973+30_3973+34dup
ENST00000644379.2:c.4096+30_4096+34dup	ENSP00000496570.2:n.4096+30_4096+34dup
ENST00000644555.2:c.647-373_647-369dup	ENSP00000494614.2:n.647-373_647-369dup
ENST00000652672.2:c.3955+30_3955+34dup	ENSP00000498906.2:n.3955+30_3955+34dup
ENST00000484087.6:c.665-373_665-369dup	ENSP00000419481.2:n.665-373_665-369dup
ENST00000700182.1:c.707-373_707-369dup	ENSP00000514849.1:n.707-373_707-369dup
ENST00000357654.9:c.4096+30_4096+34dup MANE Select	ENSP00000350283.3:n.4096+30_4096+34dup
ENST00000471181.7:c.4096+30_4096+34dup	ENSP00000418960.2:n.4096+30_4096+34dup
ENST00000644379.1:c.417+30_417+34dup
ENST00000352993.7:c.671-373_671-369dup	ENSP00000312236.5:n.671-373_671-369dup
ENST00000354071.7:c.4126_4130dup	ENSP00000326002.7:p.Ile1378SerfsTer8
ENST00000357654.7:c.4096+30_4096+34dup	ENSP00000350283.3:n.4096+30_4096+34dup
ENST00000461221.5:c.*3879+30_*3879+34dup	ENSP00000418548.1:n.*3879+30_*3879+34dup
ENST00000461574.1:c.390+30_390+34dup
ENST00000468300.5:c.788-373_788-369dup	ENSP00000417148.1:n.788-373_788-369dup
ENST00000471181.6:c.4096+30_4096+34dup	ENSP00000418960.2:n.4096+30_4096+34dup
ENST00000478531.5:c.785-373_785-369dup	ENSP00000420412.1:n.785-373_785-369dup
ENST00000484087.5:c.410-373_410-369dup	ENSP00000419481.1:n.410-373_410-369dup
ENST00000487825.5:c.413-373_413-369dup	ENSP00000418212.1:n.413-373_413-369dup
ENST00000491747.6:c.788-373_788-369dup	ENSP00000420705.2:n.788-373_788-369dup
ENST00000493795.5:c.3955+30_3955+34dup	ENSP00000418775.1:n.3955+30_3955+34dup
ENST00000493919.5:c.647-373_647-369dup	ENSP00000418819.1:n.647-373_647-369dup
ENST00000586385.5:c.5-27454_5-27450dup	ENSP00000465818.1:n.5-27454_5-27450dup
ENST00000591534.5:c.-43-16884_-43-16880dup	ENSP00000467329.1:n.-43-16884_-43-16880dup
ENST00000591849.5:c.-99+33866_-99+33870dup	ENSP00000465347.1:n.-99+33866_-99+33870dup
NM_007294.3:c.4096+30_4096+34dup , LRG_292t1:c.4096+30_4096+34dup	NP_009225.1:n.4096+30_4096+34dup
NM_007297.3:c.3955+30_3955+34dup	NP_009228.2:n.3955+30_3955+34dup
NM_007298.3:c.788-373_788-369dup	NP_009229.2:n.788-373_788-369dup
NM_007299.3:c.788-373_788-369dup	NP_009230.2:n.788-373_788-369dup
NM_007300.3:c.4096+30_4096+34dup	NP_009231.2:n.4096+30_4096+34dup
NR_027676.1:n.4232+30_4232+34dup
NM_007294.4:c.4096+30_4096+34dup MANE Select	NP_009225.1:n.4096+30_4096+34dup
NM_007297.4:c.3955+30_3955+34dup	NP_009228.2:n.3955+30_3955+34dup
NM_007299.4:c.788-373_788-369dup	NP_009230.2:n.788-373_788-369dup
NM_007300.4:c.4096+30_4096+34dup	NP_009231.2:n.4096+30_4096+34dup
NR_027676.2:n.4273+30_4273+34dup