Canonical Allele Identifier: CA10589869

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 266242
• ClinVar RCV Id: RCV000256727
• dbSNP Id: rs886040019
• MyVariant Identifiers: chr17:g.41245325_41245326del (hg19) ; chr17:g.43093308_43093309del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43093309_43093310del , CM000679.2:g.43093309_43093310del	GRCh38
NC_000017.10:g.41245326_41245327del , CM000679.1:g.41245326_41245327del	GRCh37
NC_000017.9:g.38498852_38498853del	NCBI36
NG_005905.2:g.124675_124676del , LRG_292:g.124675_124676del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.2286_2287del
ENST00000461574.2:c.2222_2223del	ENSP00000417241.2:p.Ser741Ter
ENST00000470026.6:c.2222_2223del	ENSP00000419274.2:p.Ser741Ter
ENST00000473961.6:c.2096_2097del	ENSP00000420201.2:p.Ser699Ter
ENST00000476777.6:c.2219_2220del	ENSP00000417554.2:p.Ser740Ter
ENST00000477152.6:c.2144_2145del	ENSP00000419988.2:p.Ser715Ter
ENST00000478531.6:c.784+1435_784+1436del	ENSP00000420412.2:n.784+1435_784+1436del
ENST00000489037.2:c.2144_2145del	ENSP00000420781.2:p.Ser715Ter
ENST00000493919.6:c.646+1435_646+1436del	ENSP00000418819.2:n.646+1435_646+1436del
ENST00000494123.6:c.2222_2223del	ENSP00000419103.2:p.Ser741Ter
ENST00000497488.2:c.1334_1335del	ENSP00000418986.2:p.Ser445Ter
ENST00000618469.2:c.2222_2223del	ENSP00000478114.2:p.Ser741Ter
ENST00000634433.2:c.2099_2100del	ENSP00000489431.2:p.Ser700Ter
ENST00000644379.2:c.2222_2223del	ENSP00000496570.2:p.Ser741Ter
ENST00000644555.2:c.646+1435_646+1436del	ENSP00000494614.2:n.646+1435_646+1436del
ENST00000652672.2:c.2081_2082del	ENSP00000498906.2:p.Ser694Ter
ENST00000484087.6:c.664+1435_664+1436del	ENSP00000419481.2:n.664+1435_664+1436del
ENST00000700182.1:c.706+1435_706+1436del	ENSP00000514849.1:n.706+1435_706+1436del
ENST00000357654.9:c.2222_2223del MANE Select	ENSP00000350283.3:p.Ser741Ter
ENST00000471181.7:c.2222_2223del	ENSP00000418960.2:p.Ser741Ter
ENST00000352993.7:c.671-2277_671-2276del	ENSP00000312236.5:n.671-2277_671-2276del
ENST00000354071.7:c.2222_2223del	ENSP00000326002.7:p.Ser741Ter
ENST00000357654.7:c.2222_2223del	ENSP00000350283.3:p.Ser741Ter
ENST00000461221.5:c.*2005_*2006del	ENSP00000418548.1:n.*2005_*2006del
ENST00000468300.5:c.787+1435_787+1436del	ENSP00000417148.1:n.787+1435_787+1436del
ENST00000471181.6:c.2222_2223del	ENSP00000418960.2:p.Ser741Ter
ENST00000478531.5:c.784+1435_784+1436del	ENSP00000420412.1:n.784+1435_784+1436del
ENST00000484087.5:c.409+1435_409+1436del	ENSP00000419481.1:n.409+1435_409+1436del
ENST00000487825.5:c.412+1435_412+1436del	ENSP00000418212.1:n.412+1435_412+1436del
ENST00000491747.6:c.787+1435_787+1436del	ENSP00000420705.2:n.787+1435_787+1436del
ENST00000493795.5:c.2081_2082del	ENSP00000418775.1:p.Ser694Ter
ENST00000493919.5:c.646+1435_646+1436del	ENSP00000418819.1:n.646+1435_646+1436del
ENST00000586385.5:c.5-29358_5-29357del	ENSP00000465818.1:n.5-29358_5-29357del
ENST00000591534.5:c.-43-18788_-43-18787del	ENSP00000467329.1:n.-43-18788_-43-18787del
ENST00000591849.5:c.-99+31962_-99+31963del	ENSP00000465347.1:n.-99+31962_-99+31963del
ENST00000634433.1:c.2099_2100del	ENSP00000489431.1:p.Ser700Ter
NM_007294.3:c.2222_2223del , LRG_292t1:c.2222_2223del	NP_009225.1:p.Ser741Ter
NM_007297.3:c.2081_2082del	NP_009228.2:p.Ser694Ter
NM_007298.3:c.787+1435_787+1436del	NP_009229.2:n.787+1435_787+1436del
NM_007299.3:c.787+1435_787+1436del	NP_009230.2:n.787+1435_787+1436del
NM_007300.3:c.2222_2223del	NP_009231.2:p.Ser741Ter
NR_027676.1:n.2358_2359del
NM_007294.4:c.2222_2223del MANE Select	NP_009225.1:p.Ser741Ter
NM_007297.4:c.2081_2082del	NP_009228.2:p.Ser694Ter
NM_007299.4:c.787+1435_787+1436del	NP_009230.2:n.787+1435_787+1436del
NM_007300.4:c.2222_2223del	NP_009231.2:p.Ser741Ter
NR_027676.2:n.2399_2400del