Canonical Allele Identifier: CA658824546

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 548220
• ClinVar RCV Id: RCV000661090
• dbSNP Id: rs1555592723
• MyVariant Identifiers: chr17:g.41246562_41246563insG (hg19) ; chr17:g.43094545_43094546insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43094545_43094546insG , CM000679.2:g.43094545_43094546insG	GRCh38
NC_000017.10:g.41246562_41246563insG , CM000679.1:g.41246562_41246563insG	GRCh37
NC_000017.9:g.38500088_38500089insG	NCBI36
NG_005905.2:g.123438_123439insC , LRG_292:g.123438_123439insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000354071.8:n.1049_1050insC
ENST00000461574.2:c.985_986insC	ENSP00000417241.2:p.Asn329ThrfsTer2
ENST00000470026.6:c.985_986insC	ENSP00000419274.2:p.Asn329ThrfsTer2
ENST00000473961.6:c.859_860insC	ENSP00000420201.2:p.Asn287ThrfsTer2
ENST00000476777.6:c.982_983insC	ENSP00000417554.2:p.Asn328ThrfsTer2
ENST00000477152.6:c.907_908insC	ENSP00000419988.2:p.Asn303ThrfsTer2
ENST00000478531.6:c.784+198_784+199insC	ENSP00000420412.2:n.784+198_784+199insC
ENST00000489037.2:c.907_908insC	ENSP00000420781.2:p.Asn303ThrfsTer2
ENST00000493919.6:c.646+198_646+199insC	ENSP00000418819.2:n.646+198_646+199insC
ENST00000494123.6:c.985_986insC	ENSP00000419103.2:p.Asn329ThrfsTer2
ENST00000497488.2:c.97_98insC	ENSP00000418986.2:p.Asn33ThrfsTer2
ENST00000618469.2:c.985_986insC	ENSP00000478114.2:p.Asn329ThrfsTer2
ENST00000634433.2:c.862_863insC	ENSP00000489431.2:p.Asn288ThrfsTer2
ENST00000644379.2:c.985_986insC	ENSP00000496570.2:p.Asn329ThrfsTer2
ENST00000644555.2:c.646+198_646+199insC	ENSP00000494614.2:n.646+198_646+199insC
ENST00000652672.2:c.844_845insC	ENSP00000498906.2:p.Asn282ThrfsTer2
ENST00000484087.6:c.664+198_664+199insC	ENSP00000419481.2:n.664+198_664+199insC
ENST00000700182.1:c.706+198_706+199insC	ENSP00000514849.1:n.706+198_706+199insC
ENST00000700183.1:c.*993_*994insC	ENSP00000514850.1:n.*993_*994insC
ENST00000357654.9:c.985_986insC MANE Select	ENSP00000350283.3:p.Asn329ThrfsTer2
ENST00000471181.7:c.985_986insC	ENSP00000418960.2:p.Asn329ThrfsTer2
ENST00000642945.1:c.*859_*860insC	ENSP00000495897.1:n.*859_*860insC
ENST00000652672.1:c.844_845insC	ENSP00000498906.1:p.Asn282ThrfsTer2
ENST00000352993.7:c.670+1300_670+1301insC	ENSP00000312236.5:n.670+1300_670+1301insC...
ENST00000354071.7:c.985_986insC	ENSP00000326002.7:p.Asn329ThrfsTer2
ENST00000357654.7:c.985_986insC	ENSP00000350283.3:p.Asn329ThrfsTer2
ENST00000412061.3:c.336_337insC
ENST00000461221.5:c.*768_*769insC	ENSP00000418548.1:n.*768_*769insC
ENST00000468300.5:c.787+198_787+199insC	ENSP00000417148.1:n.787+198_787+199insC
ENST00000470026.5:c.985_986insC	ENSP00000419274.1:p.Asn329ThrfsTer2
ENST00000471181.6:c.985_986insC	ENSP00000418960.2:p.Asn329ThrfsTer2
ENST00000473961.5:c.582_583insC
ENST00000477152.5:c.907_908insC	ENSP00000419988.1:p.Asn303ThrfsTer2
ENST00000478531.5:c.784+198_784+199insC	ENSP00000420412.1:n.784+198_784+199insC
ENST00000484087.5:c.409+198_409+199insC	ENSP00000419481.1:n.409+198_409+199insC
ENST00000487825.5:c.412+198_412+199insC	ENSP00000418212.1:n.412+198_412+199insC
ENST00000491747.6:c.787+198_787+199insC	ENSP00000420705.2:n.787+198_787+199insC
ENST00000492859.5:c.*921_*922insC	ENSP00000420253.1:n.*921_*922insC
ENST00000493795.5:c.844_845insC	ENSP00000418775.1:p.Asn282ThrfsTer2
ENST00000493919.5:c.646+198_646+199insC	ENSP00000418819.1:n.646+198_646+199insC
ENST00000494123.5:c.985_986insC	ENSP00000419103.1:p.Asn329ThrfsTer2
ENST00000497488.1:c.97_98insC	ENSP00000418986.1:p.Asn33ThrfsTer2
ENST00000586385.5:c.5-30595_5-30594insC	ENSP00000465818.1:n.5-30595_5-30594insC
ENST00000591534.5:c.-43-20025_-43-20024insC	ENSP00000467329.1:n.-43-20025_-43-20024in...
ENST00000591849.5:c.-99+30725_-99+30726insC	ENSP00000465347.1:n.-99+30725_-99+30726in...
ENST00000634433.1:c.862_863insC	ENSP00000489431.1:p.Asn288ThrfsTer2
NM_007294.3:c.985_986insC , LRG_292t1:c.985_986insC	NP_009225.1:p.Asn329ThrfsTer2
NM_007297.3:c.844_845insC	NP_009228.2:p.Asn282ThrfsTer2
NM_007298.3:c.787+198_787+199insC	NP_009229.2:n.787+198_787+199insC
NM_007299.3:c.787+198_787+199insC	NP_009230.2:n.787+198_787+199insC
NM_007300.3:c.985_986insC	NP_009231.2:p.Asn329ThrfsTer2
NR_027676.1:n.1121_1122insC
NM_007294.4:c.985_986insC MANE Select	NP_009225.1:p.Asn329ThrfsTer2
NM_007297.4:c.844_845insC	NP_009228.2:p.Asn282ThrfsTer2
NM_007299.4:c.787+198_787+199insC	NP_009230.2:n.787+198_787+199insC
NM_007300.4:c.985_986insC	NP_009231.2:p.Asn329ThrfsTer2
NR_027676.2:n.1162_1163insC