Canonical Allele Identifier: CA658824540

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 548292
• ClinVar RCV Id: RCV000661290
• dbSNP Id: rs1555592544
• MyVariant Identifiers: chr17:g.41246466_41246467insT (hg19) ; chr17:g.43094449_43094450insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43094449_43094450insT , CM000679.2:g.43094449_43094450insT	GRCh38
NC_000017.10:g.41246466_41246467insT , CM000679.1:g.41246466_41246467insT	GRCh37
NC_000017.9:g.38499992_38499993insT	NCBI36
NG_005905.2:g.123534_123535insA , LRG_292:g.123534_123535insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000354071.8:n.1145_1146insA
ENST00000461574.2:c.1081_1082insA	ENSP00000417241.2:p.Ser361TyrfsTer5
ENST00000470026.6:c.1081_1082insA	ENSP00000419274.2:p.Ser361TyrfsTer5
ENST00000473961.6:c.955_956insA	ENSP00000420201.2:p.Ser319TyrfsTer5
ENST00000476777.6:c.1078_1079insA	ENSP00000417554.2:p.Ser360TyrfsTer5
ENST00000477152.6:c.1003_1004insA	ENSP00000419988.2:p.Ser335TyrfsTer5
ENST00000478531.6:c.784+294_784+295insA	ENSP00000420412.2:n.784+294_784+295insA
ENST00000489037.2:c.1003_1004insA	ENSP00000420781.2:p.Ser335TyrfsTer5
ENST00000493919.6:c.646+294_646+295insA	ENSP00000418819.2:n.646+294_646+295insA
ENST00000494123.6:c.1081_1082insA	ENSP00000419103.2:p.Ser361TyrfsTer5
ENST00000497488.2:c.193_194insA	ENSP00000418986.2:p.Ser65TyrfsTer5
ENST00000618469.2:c.1081_1082insA	ENSP00000478114.2:p.Ser361TyrfsTer5
ENST00000634433.2:c.958_959insA	ENSP00000489431.2:p.Ser320TyrfsTer5
ENST00000644379.2:c.1081_1082insA	ENSP00000496570.2:p.Ser361TyrfsTer5
ENST00000644555.2:c.646+294_646+295insA	ENSP00000494614.2:n.646+294_646+295insA
ENST00000652672.2:c.940_941insA	ENSP00000498906.2:p.Ser314TyrfsTer5
ENST00000484087.6:c.664+294_664+295insA	ENSP00000419481.2:n.664+294_664+295insA
ENST00000700182.1:c.706+294_706+295insA	ENSP00000514849.1:n.706+294_706+295insA
ENST00000700183.1:c.*1089_*1090insA	ENSP00000514850.1:n.*1089_*1090insA
ENST00000357654.9:c.1081_1082insA MANE Select	ENSP00000350283.3:p.Ser361TyrfsTer5
ENST00000471181.7:c.1081_1082insA	ENSP00000418960.2:p.Ser361TyrfsTer5
ENST00000652672.1:c.940_941insA	ENSP00000498906.1:p.Ser314TyrfsTer5
ENST00000352993.7:c.670+1396_670+1397insA	ENSP00000312236.5:n.670+1396_670+1397insA...
ENST00000354071.7:c.1081_1082insA	ENSP00000326002.7:p.Ser361TyrfsTer5
ENST00000357654.7:c.1081_1082insA	ENSP00000350283.3:p.Ser361TyrfsTer5
ENST00000412061.3:c.432_433insA
ENST00000461221.5:c.*864_*865insA	ENSP00000418548.1:n.*864_*865insA
ENST00000468300.5:c.787+294_787+295insA	ENSP00000417148.1:n.787+294_787+295insA
ENST00000470026.5:c.1081_1082insA	ENSP00000419274.1:p.Ser361TyrfsTer5
ENST00000471181.6:c.1081_1082insA	ENSP00000418960.2:p.Ser361TyrfsTer5
ENST00000473961.5:c.678_679insA
ENST00000477152.5:c.1003_1004insA	ENSP00000419988.1:p.Ser335TyrfsTer5
ENST00000478531.5:c.784+294_784+295insA	ENSP00000420412.1:n.784+294_784+295insA
ENST00000484087.5:c.409+294_409+295insA	ENSP00000419481.1:n.409+294_409+295insA
ENST00000487825.5:c.412+294_412+295insA	ENSP00000418212.1:n.412+294_412+295insA
ENST00000491747.6:c.787+294_787+295insA	ENSP00000420705.2:n.787+294_787+295insA
ENST00000492859.5:c.*1017_*1018insA	ENSP00000420253.1:n.*1017_*1018insA
ENST00000493795.5:c.940_941insA	ENSP00000418775.1:p.Ser314TyrfsTer5
ENST00000493919.5:c.646+294_646+295insA	ENSP00000418819.1:n.646+294_646+295insA
ENST00000494123.5:c.1081_1082insA	ENSP00000419103.1:p.Ser361TyrfsTer5
ENST00000497488.1:c.193_194insA	ENSP00000418986.1:p.Ser65TyrfsTer5
ENST00000586385.5:c.5-30499_5-30498insA	ENSP00000465818.1:n.5-30499_5-30498insA
ENST00000591534.5:c.-43-19929_-43-19928insA	ENSP00000467329.1:n.-43-19929_-43-19928in...
ENST00000591849.5:c.-99+30821_-99+30822insA	ENSP00000465347.1:n.-99+30821_-99+30822in...
ENST00000634433.1:c.958_959insA	ENSP00000489431.1:p.Ser320TyrfsTer5
NM_007294.3:c.1081_1082insA , LRG_292t1:c.1081_1082insA	NP_009225.1:p.Ser361TyrfsTer5
NM_007297.3:c.940_941insA	NP_009228.2:p.Ser314TyrfsTer5
NM_007298.3:c.787+294_787+295insA	NP_009229.2:n.787+294_787+295insA
NM_007299.3:c.787+294_787+295insA	NP_009230.2:n.787+294_787+295insA
NM_007300.3:c.1081_1082insA	NP_009231.2:p.Ser361TyrfsTer5
NR_027676.1:n.1217_1218insA
NM_007294.4:c.1081_1082insA MANE Select	NP_009225.1:p.Ser361TyrfsTer5
NM_007297.4:c.940_941insA	NP_009228.2:p.Ser314TyrfsTer5
NM_007299.4:c.787+294_787+295insA	NP_009230.2:n.787+294_787+295insA
NM_007300.4:c.1081_1082insA	NP_009231.2:p.Ser361TyrfsTer5
NR_027676.2:n.1258_1259insA