Canonical Allele Identifier: CA059645

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 1064293
• ClinVar RCV Id: RCV001374245
• dbSNP Id: rs761640584
• ExAC: 17:41234585 T / A
• gnomAD v2: 17-41234585-T-A
• gnomAD v4: 17-43082568-T-A
• MyVariant Identifiers: chr17:g.41234585T>A (hg19) ; chr17:g.43082568T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43082568T>A , CM000679.2:g.43082568T>A	GRCh38
NC_000017.10:g.41234585T>A , CM000679.1:g.41234585T>A	GRCh37
NC_000017.9:g.38488111T>A	NCBI36
NG_005905.2:g.135416A>T , LRG_292:g.135416A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.4193A>T	ENSP00000417241.2:p.Asp1398Val
ENST00000470026.6:c.4193A>T	ENSP00000419274.2:p.Asp1398Val
ENST00000473961.6:c.4067A>T	ENSP00000420201.2:p.Asp1356Val
ENST00000476777.6:c.4187A>T	ENSP00000417554.2:p.Asp1396Val
ENST00000477152.6:c.4115A>T	ENSP00000419988.2:p.Asp1372Val
ENST00000478531.6:c.881A>T	ENSP00000420412.2:p.Asp294Val
ENST00000489037.2:c.4115A>T	ENSP00000420781.2:p.Asp1372Val
ENST00000493919.6:c.743A>T	ENSP00000418819.2:p.Asp248Val
ENST00000494123.6:c.4193A>T	ENSP00000419103.2:p.Asp1398Val
ENST00000497488.2:c.3305A>T	ENSP00000418986.2:p.Asp1102Val
ENST00000618469.2:c.4193A>T	ENSP00000478114.2:p.Asp1398Val
ENST00000634433.2:c.4070A>T	ENSP00000489431.2:p.Asp1357Val
ENST00000644379.2:c.4193A>T	ENSP00000496570.2:p.Asp1398Val
ENST00000644555.2:c.743A>T	ENSP00000494614.2:p.Asp248Val
ENST00000652672.2:c.4052A>T	ENSP00000498906.2:p.Asp1351Val
ENST00000484087.6:c.758A>T	ENSP00000419481.2:p.Asp253Val
ENST00000700182.1:c.803A>T	ENSP00000514849.1:p.Asp268Val
ENST00000357654.9:c.4193A>T MANE Select	ENSP00000350283.3:p.Asp1398Val
ENST00000471181.7:c.4193A>T	ENSP00000418960.2:p.Asp1398Val
ENST00000644379.1:c.514A>T
ENST00000352993.7:c.767A>T	ENSP00000312236.5:p.Asp256Val
ENST00000357654.7:c.4193A>T	ENSP00000350283.3:p.Asp1398Val
ENST00000461221.5:c.*3976A>T	ENSP00000418548.1:n.*3976A>T
ENST00000461574.1:c.487A>T
ENST00000468300.5:c.884A>T	ENSP00000417148.1:p.Asp295Val
ENST00000471181.6:c.4193A>T	ENSP00000418960.2:p.Asp1398Val
ENST00000478531.5:c.881A>T	ENSP00000420412.1:p.Asp294Val
ENST00000484087.5:c.506A>T	ENSP00000419481.1:p.Asp169Val
ENST00000487825.5:c.509A>T	ENSP00000418212.1:p.Asp170Val
ENST00000491747.6:c.884A>T	ENSP00000420705.2:p.Asp295Val
ENST00000493795.5:c.4052A>T	ENSP00000418775.1:p.Asp1351Val
ENST00000493919.5:c.743A>T	ENSP00000418819.1:p.Asp248Val
ENST00000586385.5:c.5-18617A>T	ENSP00000465818.1:n.5-18617A>T
ENST00000591534.5:c.-43-8047A>T	ENSP00000467329.1:n.-43-8047A>T
ENST00000591849.5:c.-98-32378A>T	ENSP00000465347.1:n.-98-32378A>T
ENST00000621897.1:n.87A>T
NM_007294.3:c.4193A>T , LRG_292t1:c.4193A>T	NP_009225.1:p.Asp1398Val
NM_007297.3:c.4052A>T	NP_009228.2:p.Asp1351Val
NM_007298.3:c.884A>T	NP_009229.2:p.Asp295Val
NM_007299.3:c.884A>T	NP_009230.2:p.Asp295Val
NM_007300.3:c.4193A>T	NP_009231.2:p.Asp1398Val
NR_027676.1:n.4329A>T
NM_007294.4:c.4193A>T MANE Select	NP_009225.1:p.Asp1398Val
NM_007297.4:c.4052A>T	NP_009228.2:p.Asp1351Val
NM_007299.4:c.884A>T	NP_009230.2:p.Asp295Val
NM_007300.4:c.4193A>T	NP_009231.2:p.Asp1398Val
NR_027676.2:n.4370A>T