Canonical Allele Identifier: CA16607667

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 389454
• ClinVar RCV Id: RCV001399289
• dbSNP Id: rs961042365
• gnomAD v3: 17-43092789-C-T
• gnomAD v4: 17-43092789-C-T
• MyVariant Identifiers: chr17:g.41244806C>T (hg19) ; chr17:g.43092789C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43092789C>T , CM000679.2:g.43092789C>T	GRCh38
NC_000017.10:g.41244806C>T , CM000679.1:g.41244806C>T	GRCh37
NC_000017.9:g.38498332C>T	NCBI36
NG_005905.2:g.125195G>A , LRG_292:g.125195G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000354071.8:n.2806G>A
ENST00000461574.2:c.2742G>A	ENSP00000417241.2:p.Glu914=
ENST00000470026.6:c.2742G>A	ENSP00000419274.2:p.Glu914=
ENST00000473961.6:c.2616G>A	ENSP00000420201.2:p.Glu872=
ENST00000476777.6:c.2739G>A	ENSP00000417554.2:p.Glu913=
ENST00000477152.6:c.2664G>A	ENSP00000419988.2:p.Glu888=
ENST00000478531.6:c.785-1757G>A	ENSP00000420412.2:n.785-1757G>A
ENST00000489037.2:c.2664G>A	ENSP00000420781.2:p.Glu888=
ENST00000493919.6:c.647-1757G>A	ENSP00000418819.2:n.647-1757G>A
ENST00000494123.6:c.2742G>A	ENSP00000419103.2:p.Glu914=
ENST00000497488.2:c.1854G>A	ENSP00000418986.2:p.Glu618=
ENST00000618469.2:c.2742G>A	ENSP00000478114.2:p.Glu914=
ENST00000634433.2:c.2619G>A	ENSP00000489431.2:p.Glu873=
ENST00000644379.2:c.2742G>A	ENSP00000496570.2:p.Glu914=
ENST00000644555.2:c.647-1757G>A	ENSP00000494614.2:n.647-1757G>A
ENST00000652672.2:c.2601G>A	ENSP00000498906.2:p.Glu867=
ENST00000484087.6:c.665-1757G>A	ENSP00000419481.2:n.665-1757G>A
ENST00000700182.1:c.707-1757G>A	ENSP00000514849.1:n.707-1757G>A
ENST00000357654.9:c.2742G>A MANE Select	ENSP00000350283.3:p.Glu914=
ENST00000471181.7:c.2742G>A	ENSP00000418960.2:p.Glu914=
ENST00000352993.7:c.671-1757G>A	ENSP00000312236.5:n.671-1757G>A
ENST00000354071.7:c.2742G>A	ENSP00000326002.7:p.Glu914=
ENST00000357654.7:c.2742G>A	ENSP00000350283.3:p.Glu914=
ENST00000461221.5:c.*2525G>A	ENSP00000418548.1:n.*2525G>A
ENST00000468300.5:c.788-1757G>A	ENSP00000417148.1:n.788-1757G>A
ENST00000471181.6:c.2742G>A	ENSP00000418960.2:p.Glu914=
ENST00000478531.5:c.785-1757G>A	ENSP00000420412.1:n.785-1757G>A
ENST00000484087.5:c.410-1757G>A	ENSP00000419481.1:n.410-1757G>A
ENST00000487825.5:c.413-1757G>A	ENSP00000418212.1:n.413-1757G>A
ENST00000491747.6:c.788-1757G>A	ENSP00000420705.2:n.788-1757G>A
ENST00000493795.5:c.2601G>A	ENSP00000418775.1:p.Glu867=
ENST00000493919.5:c.647-1757G>A	ENSP00000418819.1:n.647-1757G>A
ENST00000586385.5:c.5-28838G>A	ENSP00000465818.1:n.5-28838G>A
ENST00000591534.5:c.-43-18268G>A	ENSP00000467329.1:n.-43-18268G>A
ENST00000591849.5:c.-99+32482G>A	ENSP00000465347.1:n.-99+32482G>A
NM_007294.3:c.2742G>A , LRG_292t1:c.2742G>A	NP_009225.1:p.Glu914=
NM_007297.3:c.2601G>A	NP_009228.2:p.Glu867=
NM_007298.3:c.788-1757G>A	NP_009229.2:n.788-1757G>A
NM_007299.3:c.788-1757G>A	NP_009230.2:n.788-1757G>A
NM_007300.3:c.2742G>A	NP_009231.2:p.Glu914=
NR_027676.1:n.2878G>A
NM_007294.4:c.2742G>A MANE Select	NP_009225.1:p.Glu914=
NM_007297.4:c.2601G>A	NP_009228.2:p.Glu867=
NM_007299.4:c.788-1757G>A	NP_009230.2:n.788-1757G>A
NM_007300.4:c.2742G>A	NP_009231.2:p.Glu914=
NR_027676.2:n.2919G>A