Canonical Allele Identifier: CA059047

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 409318
• ClinVar RCV Id: RCV000467857 ; RCV000510024 ; RCV000588993
• dbSNP Id: rs775339017
• ExAC: 17:41243520 T / A
• gnomAD v2: 17-41243520-T-A
• gnomAD v3: 17-43091503-T-A
• gnomAD v4: 17-43091503-T-A
• MyVariant Identifiers: chr17:g.41243520T>A (hg19) ; chr17:g.43091503T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43091503T>A , CM000679.2:g.43091503T>A	GRCh38
NC_000017.10:g.41243520T>A , CM000679.1:g.41243520T>A	GRCh37
NC_000017.9:g.38497046T>A	NCBI36
NG_005905.2:g.126481A>T , LRG_292:g.126481A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000354071.8:n.4092A>T
ENST00000461574.2:c.4028A>T	ENSP00000417241.2:p.Asp1343Val
ENST00000470026.6:c.4028A>T	ENSP00000419274.2:p.Asp1343Val
ENST00000473961.6:c.3902A>T	ENSP00000420201.2:p.Asp1301Val
ENST00000476777.6:c.4025A>T	ENSP00000417554.2:p.Asp1342Val
ENST00000477152.6:c.3950A>T	ENSP00000419988.2:p.Asp1317Val
ENST00000478531.6:c.785-471A>T	ENSP00000420412.2:n.785-471A>T
ENST00000489037.2:c.3950A>T	ENSP00000420781.2:p.Asp1317Val
ENST00000493919.6:c.647-471A>T	ENSP00000418819.2:n.647-471A>T
ENST00000494123.6:c.4028A>T	ENSP00000419103.2:p.Asp1343Val
ENST00000497488.2:c.3140A>T	ENSP00000418986.2:p.Asp1047Val
ENST00000618469.2:c.4028A>T	ENSP00000478114.2:p.Asp1343Val
ENST00000634433.2:c.3905A>T	ENSP00000489431.2:p.Asp1302Val
ENST00000644379.2:c.4028A>T	ENSP00000496570.2:p.Asp1343Val
ENST00000644555.2:c.647-471A>T	ENSP00000494614.2:n.647-471A>T
ENST00000652672.2:c.3887A>T	ENSP00000498906.2:p.Asp1296Val
ENST00000484087.6:c.665-471A>T	ENSP00000419481.2:n.665-471A>T
ENST00000700182.1:c.707-471A>T	ENSP00000514849.1:n.707-471A>T
ENST00000357654.9:c.4028A>T MANE Select	ENSP00000350283.3:p.Asp1343Val
ENST00000471181.7:c.4028A>T	ENSP00000418960.2:p.Asp1343Val
ENST00000644379.1:c.349A>T
ENST00000352993.7:c.671-471A>T	ENSP00000312236.5:n.671-471A>T
ENST00000354071.7:c.4028A>T	ENSP00000326002.7:p.Asp1343Val
ENST00000357654.7:c.4028A>T	ENSP00000350283.3:p.Asp1343Val
ENST00000461221.5:c.*3811A>T	ENSP00000418548.1:n.*3811A>T
ENST00000461574.1:c.322A>T
ENST00000468300.5:c.788-471A>T	ENSP00000417148.1:n.788-471A>T
ENST00000471181.6:c.4028A>T	ENSP00000418960.2:p.Asp1343Val
ENST00000478531.5:c.785-471A>T	ENSP00000420412.1:n.785-471A>T
ENST00000484087.5:c.410-471A>T	ENSP00000419481.1:n.410-471A>T
ENST00000487825.5:c.413-471A>T	ENSP00000418212.1:n.413-471A>T
ENST00000491747.6:c.788-471A>T	ENSP00000420705.2:n.788-471A>T
ENST00000493795.5:c.3887A>T	ENSP00000418775.1:p.Asp1296Val
ENST00000493919.5:c.647-471A>T	ENSP00000418819.1:n.647-471A>T
ENST00000586385.5:c.5-27552A>T	ENSP00000465818.1:n.5-27552A>T
ENST00000591534.5:c.-43-16982A>T	ENSP00000467329.1:n.-43-16982A>T
ENST00000591849.5:c.-99+33768A>T	ENSP00000465347.1:n.-99+33768A>T
NM_007294.3:c.4028A>T , LRG_292t1:c.4028A>T	NP_009225.1:p.Asp1343Val
NM_007297.3:c.3887A>T	NP_009228.2:p.Asp1296Val
NM_007298.3:c.788-471A>T	NP_009229.2:n.788-471A>T
NM_007299.3:c.788-471A>T	NP_009230.2:n.788-471A>T
NM_007300.3:c.4028A>T	NP_009231.2:p.Asp1343Val
NR_027676.1:n.4164A>T
NM_007294.4:c.4028A>T MANE Select	NP_009225.1:p.Asp1343Val
NM_007297.4:c.3887A>T	NP_009228.2:p.Asp1296Val
NM_007299.4:c.788-471A>T	NP_009230.2:n.788-471A>T
NM_007300.4:c.4028A>T	NP_009231.2:p.Asp1343Val
NR_027676.2:n.4205A>T