Canonical Allele Identifier: CA10585937
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 252434
dbSNP Id: rs879255318

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43071218_43071224dup , CM000679.2:g.43071218_43071224dup GRCh38
NC_000017.10:g.41223235_41223241dup , CM000679.1:g.41223235_41223241dup GRCh37
NC_000017.9:g.38476761_38476767dup NCBI36
NG_005905.2:g.146768_146774dup , LRG_292:g.146768_146774dup

Transcript Alleles

HGVS Amino-acid change
ENST00000461574.2:c.4695_4701dup ENSP00000417241.2:p.Ser1568TrpfsTer7
ENST00000470026.6:c.4698_4704dup ENSP00000419274.2:p.Ser1569TrpfsTer7
ENST00000473961.6:c.4572_4578dup ENSP00000420201.2:p.Ser1527TrpfsTer7
ENST00000476777.6:c.4692_4698dup ENSP00000417554.2:p.Ser1567TrpfsTer7
ENST00000477152.6:c.4620_4626dup ENSP00000419988.2:p.Ser1543TrpfsTer7
ENST00000478531.6:c.1386_1392dup ENSP00000420412.2:p.Ser465TrpfsTer7
ENST00000489037.2:c.4620_4626dup ENSP00000420781.2:p.Ser1543TrpfsTer7
ENST00000493919.6:c.1248_1254dup ENSP00000418819.2:p.Ser419TrpfsTer7
ENST00000494123.6:c.4698_4704dup ENSP00000419103.2:p.Ser1569TrpfsTer7
ENST00000497488.2:c.3810_3816dup ENSP00000418986.2:p.Ser1273TrpfsTer7
ENST00000618469.2:c.4698_4704dup ENSP00000478114.2:p.Ser1569TrpfsTer7
ENST00000634433.2:c.4575_4581dup ENSP00000489431.2:p.Ser1528TrpfsTer7
ENST00000644379.2:c.4764_4770dup ENSP00000496570.2:p.Ser1591TrpfsTer7
ENST00000644555.2:c.1248_1254dup ENSP00000494614.2:p.Ser419TrpfsTer7
ENST00000652672.2:c.4557_4563dup ENSP00000498906.2:p.Ser1522TrpfsTer7
ENST00000484087.6:c.1260_1266dup ENSP00000419481.2:p.Ser423TrpfsTer7
ENST00000700182.1:c.1305_1311dup ENSP00000514849.1:p.Ser438TrpfsTer7
ENST00000357654.9:c.4698_4704dup MANE Select ENSP00000350283.3:p.Ser1569TrpfsTer7
ENST00000471181.7:c.4761_4767dup ENSP00000418960.2:p.Ser1590TrpfsTer7
ENST00000644379.1:c.1085_1091dup
ENST00000352993.7:c.1272_1278dup ENSP00000312236.5:p.Ser427TrpfsTer7
ENST00000357654.7:c.4698_4704dup ENSP00000350283.3:p.Ser1569TrpfsTer7
ENST00000461221.5:c.*4481_*4487dup ENSP00000418548.1:n.*4481_*4487dup
ENST00000468300.5:c.1386_1392dup ENSP00000417148.1:p.Ser465TrpfsTer7
ENST00000471181.6:c.4761_4767dup ENSP00000418960.2:p.Ser1590TrpfsTer7
ENST00000478531.5:c.1386_1392dup ENSP00000420412.1:p.Ser465TrpfsTer7
ENST00000484087.5:c.1011_1017dup ENSP00000419481.1:p.Ser340TrpfsTer7
ENST00000491747.6:c.1386_1392dup ENSP00000420705.2:p.Ser465TrpfsTer7
ENST00000493795.5:c.4557_4563dup ENSP00000418775.1:p.Ser1522TrpfsTer7
ENST00000493919.5:c.1248_1254dup ENSP00000418819.1:p.Ser419TrpfsTer7
ENST00000586385.5:c.5-7265_5-7259dup ENSP00000465818.1:n.5-7265_5-7259dup
ENST00000591534.5:c.171_177dup ENSP00000467329.1:p.Ser60TrpfsTer7
ENST00000591849.5:c.-98-21026_-98-21020dup ENSP00000465347.1:n.-98-21026_-98-21020dup
NM_007294.3:c.4698_4704dup , LRG_292t1:c.4698_4704dup NP_009225.1:p.Ser1569TrpfsTer7
NM_007297.3:c.4557_4563dup NP_009228.2:p.Ser1522TrpfsTer7
NM_007298.3:c.1386_1392dup NP_009229.2:p.Ser465TrpfsTer7
NM_007299.3:c.1386_1392dup NP_009230.2:p.Ser465TrpfsTer7
NM_007300.3:c.4761_4767dup NP_009231.2:p.Ser1590TrpfsTer7
NR_027676.1:n.4834_4840dup
NM_007294.4:c.4698_4704dup MANE Select NP_009225.1:p.Ser1569TrpfsTer7
NM_007297.4:c.4557_4563dup NP_009228.2:p.Ser1522TrpfsTer7
NM_007299.4:c.1386_1392dup NP_009230.2:p.Ser465TrpfsTer7
NM_007300.4:c.4761_4767dup NP_009231.2:p.Ser1590TrpfsTer7
NR_027676.2:n.4875_4881dup